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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926849Generated: October 26, 2026

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

https://huagongshe.com/reaction/926849

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 thioacetate (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, 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 numberUS09289430B2
Source datasetuspto-grants-2016_03
ORD IDord-82b2bdc6b6eb4e86ad2589512160c181
Source noteuspto-grants-2016_03