HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252376Generated: October 26, 2026
Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → Benzyl 3-(ethoxycarbonyl)-2-(2-methylpropyl)propenoate
https://huagongshe.com/reaction/1252376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester | HCID 70670 | — |
| Reactant | Benzyl 4-methyl-2-oxopentanoate | HCID 4072499 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 3-(ethoxycarbonyl)-2-(2-methylpropyl)propenoate | HCID 53921709 | 91.1% |
Reaction Steps
Ethoxycarbonylmethylenetriphenylphosphorane (53.8 g., 0.155 mol.) was dissolved in dry dichloromethane (400 mls.) and the resulting solution was cooled to 0° C. To the cooled solution was added a solution of benzyl 4-methyl-2-oxopentanoate (34.0 g., 0.155 mol.) in dry dichloromethane (100 mls.) over a period of 25 minutes and the reaction mixture was then heated under reflux for 1 hour. The solvent was removed from the reaction mixture by evaporation in vacuo to yield an off-white solid. The solid was extracted with hexane (3×200 mls.) and the solvent was removed from the combined hexane extracts to yield a crude product as a yellow oil. The crude product was purified by distillation (0.6 mm Hg), to yield E and Z benzyl 3-(ethoxycarbonyl)-2-(2-methylpropyl)propenoate (41.0 g.) being collected at 137°-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04743587 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-f8f072e0442e4efc9337b0b8dc4d4a04 |
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| Source note | uspto-grants-1988_05 |
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