Reaction #4132014
Related Literature (1)
openreactiondata ↗doi:10.1039/C8SC04228D
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-5e51c7975bc34a5085cde80049ffa2d7No renderable structure data available
CCOC(=O)C=C1CCC1Chemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | ethyl 2-cyclobutylideneacetate |
|---|---|
| IUPAC Name | — |
| CAS Number | 27741-65-7 |
| Database ID | 15724666 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
ethyl 2-cyclobutylideneacetate (CAS 27741-65-7) 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 15724666
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-5e51c7975bc34a5085cde80049ffa2d7Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-5622b48d92334f3e8b38291643dcbcddConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-33e19d521f7449839b4f91c15edc05c0Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-2bdeb80b77ab4408a7cc8a4504342563Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The unsaturated ester (2) (5.79 g, 41.4 mmol) was dissolved in tetrahydrofuran (20 mL) and stirred at 70° C. with nitromethane (4.67 mL, 86.4 mmol) and tetrabutylammonium fluoride (1.0 M in tetrahydrofuran, 55 mL, 55.0 mmol). After 18 hours, the mixture was cooled to room temperature, diluted with ethyl acetate (150 mL), and washed with 2N HCl (60 mL) followed by brine (100 mL). The organic phase was collected, dried (MgSO4), and the solvent removed in vacuo. The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1) to give 4.34 g (52%) of a clear oil. washed with 2N HCl (60 mL) The organic phase was collected dried (MgSO4) the solvent removed in vacuo The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1)
Source ID: ord-018f0f0cbc414716bc95ff1046ea1805Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The unsaturated ester (2) (5.79 g, 41.4 mmol) was dissolved in tetrahydrofuran (20 mL) and stirred at 70° C. with nitromethane (4.67 mL, 86.4 mmol) and tetrabutylammonium fluoride (1.0 M in tetrahydrofuran, 55 mL, 55.0 mmol). After 18 hours, the mixture was cooled to room temperature, diluted with ethyl acetate (150 mL), and washed with 2N HCl (60 mL) followed by brine (100 mL). The organic phase was collected, dried (MgSO4), and the solvent removed in vacuo. The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1) to give 4.34 g (52%) of a clear oil. washed with 2N HCl (60 mL) The organic phase was collected dried (MgSO4) the solvent removed in vacuo The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1)
Source ID: ord-018f0f0cbc414716bc95ff1046ea1805Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The unsaturated ester (2) (5.79 g, 41.4 mmol) was dissolved in tetrahydrofuran (20 mL) and stirred at 70° C. with nitromethane (4.67 mL, 86.4 mmol) and tetrabutylammonium fluoride (1.0 M in tetrahydrofuran, 55 mL, 55.0 mmol). After 18 hours, the mixture was cooled to room temperature, diluted with ethyl acetate (150 mL), and washed with 2N HCl (60 mL) followed by brine (100 mL). The organic phase was collected, dried (MgSO4), and the solvent removed in vacuo. The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1) to give 4.34 g (52%) of a clear oil. washed with 2N HCl (60 mL) The organic phase was collected dried (MgSO4) the solvent removed in vacuo The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1)
Source ID: ord-df629faf40af426fab363e568fffe13aConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The unsaturated ester (2) (5.79 g, 41.4 mmol) was dissolved in tetrahydrofuran (20 mL) and stirred at 70° C. with nitromethane (4.67 mL, 86.4 mmol) and tetrabutylammonium fluoride (1.0 M in tetrahydrofuran, 55 mL, 55.0 mmol). After 18 hours, the mixture was cooled to room temperature, diluted with ethyl acetate (150 mL), and washed with 2N HCl (60 mL) followed by brine (100 mL). The organic phase was collected, dried (MgSO4), and the solvent removed in vacuo. The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1) to give 4.34 g (52%) of a clear oil. washed with 2N HCl (60 mL) The organic phase was collected dried (MgSO4) the solvent removed in vacuo The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1)
Source ID: ord-df629faf40af426fab363e568fffe13aConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-5e51c7975bc34a5085cde80049ffa2d7Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-5622b48d92334f3e8b38291643dcbcddConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-33e19d521f7449839b4f91c15edc05c0Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-2bdeb80b77ab4408a7cc8a4504342563PubChem References
These sources are listed in the compound's public database record.
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