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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407947Generated: October 26, 2026

3-(Bromomethyl)benzoic acid → 3-(Acetylthiomethyl)benzoic acid

https://huagongshe.com/reaction/1407947

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Bromomethyl)benzoic acidHCID 245650—
ReactantPotassium ethanethioateHCID 23670855—
SolventEthanolHCID 702—
Product3-(Acetylthiomethyl)benzoic acidHCID 86089206—

Reaction Steps

Into a 250-mL round-bottom flask, was placed a solution of 3-(bromomethyl)benzoic acid (7 g, 32.56 mmol, 1.00 equiv) in ethanol (80 mL), and potassium ethanethioate (9.65 g, 84.65 mmol, 2.60 equiv). The resulting solution was stirred overnight at room temperature. The resulting mixture was concentrated under vacuum. The resulting solution was diluted with 80 mL of water and adjusted to pH 3-4 with 10% hydrochloric acid. The resulting solution was extracted with 3×50 mL of ethyl acetate and the organic layers combined. The resulting mixture was washed with 1×50 mL of brine. The mixture was dried over sodium sulfate and concentrated under vacuum. This resulted in 4.4 g (64%) of 3-(acetylthiomethyl)benzoic acid as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916569B2
Source datasetuspto-grants-2014_12
ORD IDord-e3b795d7510c49f59fb2e43241e3f0a3
Source noteuspto-grants-2014_12