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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365047Generated: October 30, 2026

Methyl 4-Formylbenzoate → 4-(Phenyl-1-butenyl)benzoic acid, methyl ester

https://huagongshe.com/reaction/365047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-FormylbenzoateHCID 15294—
Reactant3-Phenylpropyl triphenylphosphonium bromideHCID 10928647—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(Phenyl-1-butenyl)benzoic acid, methyl esterHCID 54000744—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° solution of phenylpropyl triphenylphosphonium bromide (3.55 g, 1.25 eq) in 30 ml of dry THF under argon was added K-t-amylate (3.9 ml, 1.1 eq). After stirring for 30 minutes at 0° C. then allowing to warm to room temperature, a solution of 4-formylbenzoic acid methyl ester (1.0 g, 6.1 mmol) in ~8 ml of dry THF was added dropwise. This solution was stirred for 3 hours at room temperature, then diluted with ~1 ml of H2O, and concentrated to remove most of the THF. EtOAc (~200 ml) was added and the mixture was washed with H2O, 1N HCl (2×) and brine. After drying over anhydrous MgSO4, the solvent was removed in vacuo to yield a yellow oil which solidified soon after. Column purification of this crude product was done on a 50 mm column on silica gel eluted with 95:5 hexane/EtOAc. Product containing fractions were combined to yield after concentration title compound, 1.5 g (93%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04607053
Source datasetuspto-grants-1986_08
ORD IDord-e7eb046364194948818c9999a268ad93
Source noteuspto-grants-1986_08