Reaction #4094180
Related Literature (1)
openreactiondata ↗doi:10.1039/C8SC04228D
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-1dfec7d636924818b7ea717c072de95dNo renderable structure data available
CCCCCCCCCCSCCOChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 2-decylsulfanylethanol |
|---|---|
| IUPAC Name | — |
| CAS Number | 41891-88-7 |
| Database ID | 96654 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
2-decylsulfanylethanol (CAS 41891-88-7) 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 96654
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
12 reactions · 12 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-1dfec7d636924818b7ea717c072de95dConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-4f9c27ad64484a52a344e95861c54b3eConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Under nitrogen, to a suspension of potassium carbonate (27 g, 200 mmol) in acetone (100 ml) was added decyl bromide (10 ml, 50 mmol) and mercaptoethanol (4.4 ml, 63 mmol). The suspension was stirred at room temperature for 2 days, then partitioned between water and 80% hexane/ethyl acetate. The organic phase was washed with 2N sodium hydroxide, dried over magnesium sulfate, and the volatiles removed under vacuum to give 2-(decylthio)ethanol (10.2 g, 47 mmol) as a colorless liquid that was used without further purification. partitioned between water and 80% hexane/ethyl acetate The organic phase was washed with 2N sodium hydroxide dried over magnesium sulfate the volatiles removed under vacuum
Source ID: ord-76c4d5abcd4a4f9a8133463c6905d816Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Under nitrogen, to a suspension of potassium carbonate (27 g, 200 mmol) in acetone (100 ml) was added decyl bromide (10 ml, 50 mmol) and mercaptoethanol (4.4 ml, 63 mmol). The suspension was stirred at room temperature for 2 days, then partitioned between water and 80% hexane/ethyl acetate. The organic phase was washed with 2N sodium hydroxide, dried over magnesium sulfate, and the volatiles removed under vacuum to give 2-(decylthio)ethanol (10.2 g, 47 mmol) as a colorless liquid that was used without further purification. partitioned between water and 80% hexane/ethyl acetate The organic phase was washed with 2N sodium hydroxide dried over magnesium sulfate the volatiles removed under vacuum
Source ID: ord-590a1b44035d459aa318292819287c6eConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Under nitrogen, to a suspension of potassium carbonate (27 g, 200 nimrnol) in acetone (100 ml) was added decyl bromide (10 ml, 50 mmol) and mercaptoethanol (4.4 ml, 63 mmol). The suspension was stirred at room temperature for 2 days, then partitioned between water and 80% hexane/ethyl acetate. The organic phase was washed with 2N sodium hydroxide, dried over magnesium sulfate, and the volatiles removed under vacuum to give 2-(decylthio)ethanol (10.2 g, 47 mmol) as a colorless liquid that was used without further purification. partitioned between water and 80% hexane/ethyl acetate The organic phase was washed with 2N sodium hydroxide dried over magnesium sulfate the volatiles removed under vacuum
Source ID: ord-6e2a91da95a74ec6ad5f0af03558996fConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Under nitrogen, to a suspension of potassium carbonate (27 g, 200 nimrnol) in acetone (100 ml) was added decyl bromide (10 ml, 50 mmol) and mercaptoethanol (4.4 ml, 63 mmol). The suspension was stirred at room temperature for 2 days, then partitioned between water and 80% hexane/ethyl acetate. The organic phase was washed with 2N sodium hydroxide, dried over magnesium sulfate, and the volatiles removed under vacuum to give 2-(decylthio)ethanol (10.2 g, 47 mmol) as a colorless liquid that was used without further purification. partitioned between water and 80% hexane/ethyl acetate The organic phase was washed with 2N sodium hydroxide dried over magnesium sulfate the volatiles removed under vacuum
Source ID: ord-6e2a91da95a74ec6ad5f0af03558996fConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Under nitrogen, to a suspension of potassium carbonate (27 g, 200 mmol) in acetone (100 ml) was added decyl bromide (10 ml, 50 mmol) and mercaptoethanol (4.4 ml, 63 mmol). The suspension was stirred at room temperature for 2 days, then partitioned between water and 80% hexane/ethyl acetate. The organic phase was washed with 2N sodium hydroxide, dried over magnesium sulfate, and the volatiles removed under vacuum to give 2-(decylthio)ethanol (10.2 g, 47 mmol) as a colorless liquid that was used without further purification. partitioned between water and 80% hexane/ethyl acetate The organic phase was washed with 2N sodium hydroxide dried over magnesium sulfate the volatiles removed under vacuum
Source ID: ord-24dbeb6e265a4ed7b39cedbceee8a220Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Under nitrogen, to a suspension of potassium carbonate (27 g, 200 mmol) in acetone (100 ml) was added decyl bromide (10 ml, 50 mmol) and mercaptoethanol (4.4 ml, 63 mmol). The suspension was stirred at room temperature for 2 days, then partitioned between water and 80% hexane/ethyl acetate. The organic phase was washed with 2N sodium hydroxide, dried over magnesium sulfate, and the volatiles removed under vacuum to give 2-(decylthio)ethanol (10.2 g, 47 mmol) as a colorless liquid that was used without further purification. partitioned between water and 80% hexane/ethyl acetate The organic phase was washed with 2N sodium hydroxide dried over magnesium sulfate the volatiles removed under vacuum
Source ID: ord-24dbeb6e265a4ed7b39cedbceee8a220Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Under nitrogen, to a suspension of potassium carbonate (27 g, 200 mmol) in acetone (100 ml) was added decyl bromide (10 ml, 50 mmol) and mercaptoethanol (4.4 ml, 63 mmol). The suspension was stirred at room temperature for 2 days, then partitioned between water and 80% hexane/ethyl acetate. The organic phase was washed with 2N sodium hydroxide, dried over magnesium sulfate, and the volatiles removed under vacuum to give 2-(decylthio)ethanol (10.2 g, 47 mmol) as a colorless liquid that was used without further purification. partitioned between water and 80% hexane/ethyl acetate The organic phase was washed with 2N sodium hydroxide dried over magnesium sulfate the volatiles removed under vacuum
Source ID: ord-145393533a6f486480d6ad898ddc5c64Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Under nitrogen, to a suspension of potassium carbonate (27 g, 200 mmol) in acetone (100 ml) was added decyl bromide (10 ml, 50 mmol) and mercaptoethanol (4.4 ml, 63 mmol). The suspension was stirred at room temperature for 2 days, then partitioned between water and 80% hexane/ethyl acetate. The organic phase was washed with 2N sodium hydroxide, dried over magnesium sulfate, and the volatiles removed under vacuum to give 2-(decylthio)ethanol (10.2 g, 47 mmol) as a colorless liquid that was used without further purification. partitioned between water and 80% hexane/ethyl acetate The organic phase was washed with 2N sodium hydroxide dried over magnesium sulfate the volatiles removed under vacuum
Source ID: ord-145393533a6f486480d6ad898ddc5c64Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Under nitrogen, to a suspension of potassium carbonate (27 g, 200 mmol) in acetone (100 ml) was added decyl bromide (10 ml, 50 mmol) and mercaptoethanol (4.4 ml, 63 mmol). The suspension was stirred at room temperature for 2 days, then partitioned between water and 80% hexane/ethyl acetate. The organic phase was washed with 2N sodium hydroxide, dried over magnesium sulfate, and the volatiles removed under vacuum to give 2-(decylthio)ethanol (10.2 g, 47 mmol) as a colorless liquid that was used without further purification. partitioned between water and 80% hexane/ethyl acetate The organic phase was washed with 2N sodium hydroxide dried over magnesium sulfate the volatiles removed under vacuum
Source ID: ord-f211ec62c4cf4933a9d3211df45c9d62Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Under nitrogen, to a suspension of potassium carbonate (27 g, 200 mmol) in acetone (100 ml) was added decyl bromide (10 ml, 50 mmol) and mercaptoethanol (4.4 ml, 63 mmol). The suspension was stirred at room temperature for 2 days, then partitioned between water and 80% hexane/ethyl acetate. The organic phase was washed with 2N sodium hydroxide, dried over magnesium sulfate, and the volatiles removed under vacuum to give 2-(decylthio)ethanol (10.2 g, 47 mmol) as a colorless liquid that was used without further purification. partitioned between water and 80% hexane/ethyl acetate The organic phase was washed with 2N sodium hydroxide dried over magnesium sulfate the volatiles removed under vacuum
Source ID: ord-f211ec62c4cf4933a9d3211df45c9d62PubChem References
These sources are listed in the compound's public database record.
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