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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
ReactantBenzyl 4-methyl-2-oxopentanoateHCID 4072499—
SolventDichloromethaneHCID 6344—
ProductBenzyl 3-(ethoxycarbonyl)-2-(2-methylpropyl)propenoateHCID 5392170991.1%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04743587
Source datasetuspto-grants-1988_05
ORD IDord-f8f072e0442e4efc9337b0b8dc4d4a04
Source noteuspto-grants-1988_05