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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261787Generated: October 26, 2026

Methyl 4-Formylbenzoate → Methyl 4-(2-methoxyethenyl)benzoate

https://huagongshe.com/reaction/2261787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-FormylbenzoateHCID 15294—
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(2-methoxyethenyl)benzoateHCID 5413664180.2%

Reaction Steps

To an ambient temperature suspension of potassium tert-butoxide (2.05 g, 18.27 mmol) in THF (60 mL) is added the (methoxymethyl)triphenyl phosphonium chloride (6.26 g, 18.27 mmol). The reaction mixture is stirred at room temperature for 20 min. Solid methyl 4-formylbenzoate (1.0 g, 6.09 mmol) is added and the reaction is stirred at room temperature overnight. The reaction mixture is quenched with saturated aq. NH4Cl and concentrated. The residue is partitioned between Et2O and water. The aqueous layer is extracted with Et2O and the combined organic layers are washed with brine, dried (MgSO4), filtered, concentrated, and chromatographed (0% to 30% EtOAC/Hex) to yield the title compound (939 mg, 80%) as a mix of E/Z isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846960B2
Source datasetuspto-grants-2010_12
ORD IDord-700444a7c81b4b9faf7ceb5b8ab3e0d9
Source noteuspto-grants-2010_12