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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789001Generated: November 2, 2026

Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → HCID 367206, compound

https://huagongshe.com/reaction/1789001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
Reactant2-BromobenzaldehydeHCID 81129—
SolventDichloromethaneHCID 6344—
ProductHCID 367206HCID 36720696%

Reaction Steps

Carboethoxymethylidene triphenylphosphorane (94 g, 270 mM) was dissolved in 350 ml of methylenechloride under nitrogen. o-Bromobenzaldehyde (31.5 ml; 270 mM) was added via an addition funnel in 125 ml of methylene chloride. The solution was allowed to stand at room temperature overnight and then the solvent was removed in vacuo. The slushy residue was taken up in 10% ethyl acetate in hexane and filtered through a one-inch pad of silica gel in a 350 ml fritted funnel with one liter of 10% ethyl acetate in hexane. Solvent removal on the rotary evaporator followed by pumping overnight gave 66.3 g of an oil, ethyl o-bromocinnamate in 96% yield. The NMR indicates a 4.5 to 1 mixture of trans to cis isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04686235
Source datasetuspto-grants-1987_08
ORD IDord-62976ea3d11749a087501c01286cd7b6
Source noteuspto-grants-1987_08