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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428714Generated: October 26, 2026

Methyl 4-Formylbenzoate → Methyl 4-ethenylbenzoate

https://huagongshe.com/reaction/428714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-FormylbenzoateHCID 15294—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventDiethyl EtherHCID 3283—
ProductMethyl 4-ethenylbenzoateHCID 583124—

Reaction Steps

To a stirred solution of n-butyllithium (4 mL, 2,5 M solution in hexane, 10 mmol) (Aldrich) in ether (30 mL) was added methyltriphenylphosphonium bromide (3.57 g, 10 mmol) (Aldrich) over a period of 5 min. The reaction mixture was stirred for 4 h at room temperature. To the resulting orange solution was added methyl 4-formylbenzoate (1.54 mL, 10 mmol) dropwise. The solution became colorless, and a white precipitate separated. The mixture was then heated to reflux and immediately allowed to cool to room temperature. The precipitate was removed by filtration. The resulting precipitate was washed with ether, and the combined ethereal filtrates were washed with water until neutral and then dried over anhydrous MgSO4. The solvent was removed and the residue, 4-ethenyl-benzoic acid methyl ester, was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313310B1
Source datasetuspto-grants-2001_11
ORD IDord-8693104f274b45b6a1977f38b376508b
Source noteuspto-grants-2001_11