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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841785Generated: October 30, 2026

Benzyl Alcohol → 2-Benzyloxy-3-methoxybenzoic acid methyl ester

https://huagongshe.com/reaction/841785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl 3-methoxysalicylateHCID 80651—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Benzyloxy-3-methoxybenzoic acid methyl esterHCID 6989164058.2%

Reaction Steps

To a solution of methyl 3-methoxysalicylate (1.0 g, 5.49 mmol) in 5 ml tetrahydrofuran and 5 ml dimethylformamide was added sequentially at room temperature, benzyl alcohol (0.71 ml, 6.86 mmol), triphenylphosphine (2.16 g, 8.23 mmol) and diethyl azodicarboxylate (1.3 ml, 8.23 mmol). The reaction solution was stirred at room temperature overnight, then ethyl acetate was added and the resulting solution was washed sequentially with water and brine. The ethyl acetate solution was dried over anhydrous sodium sulfate and concentrated to dryness in vacuo. The residue was triturated with diethyl ether and filtered to remove triphenylphosphine oxide. The ether solution was concentrated to dryness in vacuo and the residue was purified by column chromatography on silica gel, eluting with 95:5 hexane/ethyl acetate, yielding the title compound as an oil (870 mg 58% yield). MS (M+1)+273.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369075B1
Source datasetuspto-grants-2002_04
ORD IDord-ca4fb8f88bff4678b867e64b7063c2e3
Source noteuspto-grants-2002_04