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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016183Generated: October 25, 2026

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

https://huagongshe.com/reaction/1016183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methoxycarbonyl)benzoic acidHCID 601880—
SolventTetrahydrofuranHCID 8028—
ProductBenzoic acid, 3-(hydroxymethyl)-, methyl esterHCID 15505887.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-(methoxycarbonyl)benzoic acid (1.05 g, 5.83 mmol) in THF (25 mL) was cooled to 0° C., and treated with the dropwise addition of 2.0 M borane-methylsulfide complex in THF (14.57 mL, 29.1 mmol) at a rate which did not allow the temperature to exceed 5° C. The mixture was stirred at 0° C. for 15 minutes, then allowed to warm to room temperature and stirred for 4 hours. The reaction was cooled to 0° C. and quenched with the addition of small pieces of ice, causing vigorous gas evolution. When gas evolution had ceased, the mixture was diluted with brine and extracted 3× with ethyl acetate. The combined organic phases were washed 3× with dilute bleach to remove residual methyl sulfide, 3× with saturated sodium carbonate to remove any unreacted acid, 1× with water, and 1× with brine, then dried over sodium sulfate and concentrated in vacuo to yield the title compound (845 mg, 5.09 mmol, 87% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985861B2
Source datasetuspto-grants-2011_07
ORD IDord-f8290a5193d64234a1f4224c4318362f
Source noteuspto-grants-2011_07