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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175250Generated: October 30, 2026

3-(Methoxycarbonyl)benzoic acid → Benzoic acid, 3-(hydroxymethyl)-, methyl ester

https://huagongshe.com/reaction/2175250

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methoxycarbonyl)benzoic acidHCID 601880—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductBenzoic acid, 3-(hydroxymethyl)-, methyl esterHCID 15505886.7%

Reaction Steps

To a solution of 3-(methoxycarbonyl)benzoic acid (0.200 g, 1.11 mmol) in THF (6.0 mL) at 0° C. was added borane tetrahydrofuran complex (5.55 mL, 5.55 mmol) slowly. The reaction mixture was slowly warmed to room temperature and stirred at for 3 h. After this time, the reaction mixture was diluted with EtOAc and quenched very slowly with water. The organic layer was separated, washed with water and brine, dried over anhydrous MgSO4, filtered, and concentrated to afford the title compound (0.16 g, 84% yield) as a colorless oil. LCMS, [M+H]+=167.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062028B2
Source datasetuspto-grants-2015_06
ORD IDord-8010e90db90844e0868ee85e91da6c98
Source noteuspto-grants-2015_06