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C1SCSCS1Chemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 1,3,5-trithiane |
|---|---|
| IUPAC Name | — |
| CAS Number | 291-21-4 |
| Database ID | 9264 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
1,3,5-trithiane (CAS 291-21-4) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
Potential Applications
For professional research and industrial use only
Database ID 9264
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
9 reactions · 9 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-3e0b035a97d542279763bbfd8dd07f86Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-3e0b035a97d542279763bbfd8dd07f86Conditions: temp:-60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: In 30 ml of anhydrous tetrahydrofuran was suspended 2.6 g of 1,3,5-trithiane, and 12 ml of 1.6M n-butyl lithium was added dropwise under an argon atmosphere at a temperature of about -20° C. After completion of the dropwise addition, the resulting mixture was stirred for 2 hours. Next, the reaction mixture was cooled to about -60° C., and then a solution of 4.0 g of 4-phenoxyacetophenone dissolved in 10 ml of tetrahydrofuran was dropped thereinto. After completion of the dropping, the reaction temperature was slowly raised to 0° C. The mixture thus obtained was stirred at 0° C. for another 1 hour. Thereafter, the same treatment as in Example 1 was carried out to obtain a crude product, which was then purified by a silica gel column chromatography (chloroform) to give 3.4 g of the desired compound. was added dropwise under an argon atmosphere at a temperature of about -20° C After completion of the dropwise addition was dropped After completion of the dropping, the reaction temperature was slowly raised to 0° C The mixture thus obtained was stirred at 0° C. for another 1 hour to obtain a crude product, which was then purified by a silica gel column chromatography (chloroform)
Source ID: ord-16ba98998bca43b5b108e5d9646c706cConditions: temp:-60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: In 30 ml of anhydrous tetrahydrofuran was suspended 2.6 g of 1,3,5-trithiane, and 12 ml of 1.6M n-butyl lithium was added dropwise under an argon atmosphere at a temperature of about -20° C. After completion of the dropwise addition, the resulting mixture was stirred for 2 hours. Next, the reaction mixture was cooled to about -60° C., and then a solution of 4.0 g of 4-phenoxyacetophenone dissolved in 10 ml of tetrahydrofuran was dropped thereinto. After completion of the dropping, the reaction temperature was slowly raised to 0° C. The mixture thus obtained was stirred at 0° C. for another 1 hour. Thereafter, the same treatment as in Example 1 was carried out to obtain a crude product, which was then purified by a silica gel column chromatography (chloroform) to give 3.4 g of the desired compound. was added dropwise under an argon atmosphere at a temperature of about -20° C After completion of the dropwise addition was dropped After completion of the dropping, the reaction temperature was slowly raised to 0° C The mixture thus obtained was stirred at 0° C. for another 1 hour to obtain a crude product, which was then purified by a silica gel column chromatography (chloroform)
Source ID: ord-16ba98998bca43b5b108e5d9646c706cConditions: temp:-60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: In 30 ml of anhydrous tetrahydrofuran was suspended 2.6 g of 1,3,5-trithiane, and 12 ml of 1.6M n-bytyl lithium was added dropwise under an argon atmosphere at a temperature of about -20° C. After completion of the dropwise addition, the resulting mixture was stirred for 2 hours. Next, the reaction mixture was cooled to about -60° C., and then a solution of 4.4 g of 4,4'-difluorobenzophenone dissolved in 100 ml of tetrahydrofuran was dropped thereinto. After completion of the dropping, the reaction temperature was slowly raised to 0° C. After stirring at 0° C. for another 1 hour, the reaction mixture thus obtained was poured into ice water and the resulting mixture was extracted with chloroform. The extract was washed with a saturated aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The crude product thus obtained was recrystallized from ether-hexane to give 5.58 g of the desired compound. was added dropwise under an argon atmosphere at a temperature of about -20° C After completion of the dropwise addition was dropped After completion of the dropping, the reaction temperature was slowly raised to 0° C After stirring at 0° C. for another 1 hour the reaction mixture thus obtained the resulting mixture was extracted with chloroform The extract was washed with a saturated aqueous sodium chloride solution dried over anhydrous magnesium sulfate the solvent was removed by distillation under reduced pressure The crude product thus obtained was recrystallized from ether-hexane
Source ID: ord-b504bba695ac49bbbb847108858f9d86Conditions: temp:-60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: In 30 ml of anhydrous tetrahydrofuran was suspended 2.6 g of 1,3,5-trithiane, and 12 ml of 1.6M n-butyl lithium was added dropwise under an argon atmosphere at a temperature of about -20° C. After completion of the dropwise addition, the resulting mixture was stirred for 2 hours. Next, the reaction mixture was cooled to about -60° C., and then a solution of 4.0 g of 4-phenoxyacetophenone dissolved in 10 ml of tetrahydrofuran was dropped thereinto. After completion of the dropping, the reaction temperature was slowly raised to 0° C. The mixture thus obtained was stirred at 0° C. for another 1 hour. Thereafter, the same treatment as in Example 1 was carrid out to obtain a crude product, which was then purified by a silica gel column chromatography (chloroform) to give 3.4 g of the desired compound. was added dropwise under an argon atmosphere at a temperature of about -20° C After completion of the dropwise addition was dropped After completion of the dropping, the reaction temperature was slowly raised to 0° C The mixture thus obtained was stirred at 0° C. for another 1 hour to obtain a crude product, which was then purified by a silica gel column chromatography (chloroform)
Source ID: ord-7b99a0a094014b1ea17e447ca7b37ca2Conditions: temp:-60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: In 30 ml of anhydrous tetrahydrofuran was suspended 2.6 g of 1,3,5-trithiane, and 12 ml of 1.6M n-bytyl lithium was added dropwise under an argon atmosphere at a temperature of about -20° C. After completion of the dropwise addition, the resulting mixture was stirred for 2 hours. Next, the reaction mixture was cooled to about -60° C., and then a solution of 4.4 g of 4,4'-difluorobenzophenone dissolved in 100 ml of tetrahydrofuran was dropped thereinto. After completion of the dropping, the reaction temperature was slowly raised to 0° C. After stirring at 0° C. for another 1 hour, the reaction mixture thus obtained was poured into ice water and the resulting mixture was extracted with chloroform. The extract was washed with a saturated aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The crude product thus obtained was recrystallized from ether-hexane to give 5.58 g of the desired compound. was added dropwise under an argon atmosphere at a temperature of about -20° C After completion of the dropwise addition was dropped After completion of the dropping, the reaction temperature was slowly raised to 0° C After stirring at 0° C. for another 1 hour the reaction mixture thus obtained the resulting mixture was extracted with chloroform The extract was washed with a saturated aqueous sodium chloride solution dried over anhydrous magnesium sulfate the solvent was removed by distillation under reduced pressure The crude product thus obtained was recrystallized from ether-hexane
Source ID: ord-2b0b1f81f7bf41a88f7434cf1ae8dfddConditions: temp:-60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: In 30 ml of anhydrous tetrahydrofuran was suspended 2.6 g of 1,3,5-trithiane, and 12 ml of 1.6M n-butyl lithium was added dropwise under an argon atmosphere at a temperature of about -20° C. After completion of the dropwise addition, the resulting mixture was stirred for 2 hours. Next, the reaction mixture was cooled to about -60° C., and then a solution of 4.0 g of 4-phenoxyacetophenone dissolved in 10 ml of tetrahydrofuran was dropped thereinto. After completion of the dropping, the reaction temperature was slowly raised to 0° C. The mixture thus obtained was stirred at 0° C. for another 1 hour. Thereafter, the same treatment as in Example 1 was carried out to obtain a crude product, which was then purified by a silica gel column chromatography (chloroform) to give 3.4 g of the desired compound. was added dropwise under an argon atmosphere at a temperature of about -20° C After completion of the dropwise addition was dropped After completion of the dropping, the reaction temperature was slowly raised to 0° C The mixture thus obtained was stirred at 0° C. for another 1 hour to obtain a crude product, which was then purified by a silica gel column chromatography (chloroform)
Source ID: ord-16ba98998bca43b5b108e5d9646c706cConditions: temp:-60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: In 30 ml of anhydrous tetrahydrofuran was suspended 2.6 g of 1,3,5-trithiane, and 12 ml of 1.6M n-bytyl lithium was added dropwise under an argon atmosphere at a temperature of about -20° C. After completion of the dropwise addition, the resulting mixture was stirred for 2 hours. Next, the reaction mixture was cooled to about -60° C., and then a solution of 4.4 g of 4,4'-difluorobenzophenone dissolved in 100 ml of tetrahydrofuran was dropped thereinto. After completion of the dropping, the reaction temperature was slowly raised to 0° C. After stirring at 0° C. for another 1 hour, the reaction mixture thus obtained was poured into ice water and the resulting mixture was extracted with chloroform. The extract was washed with a saturated aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The crude product thus obtained was recrystallized from ether-hexane to give 5.58 g of the desired compound. was added dropwise under an argon atmosphere at a temperature of about -20° C After completion of the dropwise addition was dropped After completion of the dropping, the reaction temperature was slowly raised to 0° C After stirring at 0° C. for another 1 hour the reaction mixture thus obtained the resulting mixture was extracted with chloroform The extract was washed with a saturated aqueous sodium chloride solution dried over anhydrous magnesium sulfate the solvent was removed by distillation under reduced pressure The crude product thus obtained was recrystallized from ether-hexane
Source ID: ord-b504bba695ac49bbbb847108858f9d86PubChem References
These sources are listed in the compound's public database record.
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