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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187626Generated: October 31, 2026

Methanol → 4-(4-Fluorophenethyl)-3-methoxycarbonylbenzoic acid

https://huagongshe.com/reaction/2187626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-DioxaneHCID 31275—
ReactantMethyl 4-(4-fluorophenethyl)-3-methoxycarbonylbenzoateHCID 18474597—
SolventWaterHCID 962—
Product4-(4-Fluorophenethyl)-3-methoxycarbonylbenzoic acidHCID 1847463686.2%

Reaction Steps

A mixture of methyl 4-(4-fluorophenethyl)-3-methoxycarbonylbenzoate (51.00 g., 161.22 mmol), dioxane (650 ml), methanol (650 ml), sodium hydroxide (7.10 g., 177.35 mmol) and water (100 ml) was stirred at ambient temperature under an inert atmosphere for 16 hours. The reaction was evaporated to dryness, water (500 ml) was added to the residue and the mixture extracted with diethyl ether. The organic extracts were dried and evaporated to dryness to give recovered methyl 4-(4-fluorophenethyl)-3-methoxycarbonylbenzoate (7 g). The aqueous layer was acidified to pH 2 with 2M HCl (300 ml) and extracted with ethyl acetate (300 ml). The organic extracts were dried, filtered and evaporated to dryness to give as a white solid 4-(4-fluorophenethyl)-3-methoxycarbonylbenzoic acid (42.00 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410539B1
Source datasetuspto-grants-2002_06
ORD IDord-b6e58b12598f4569ae7ea73506a7f4aa
Source noteuspto-grants-2002_06