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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409826Generated: November 1, 2026

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

https://huagongshe.com/reaction/2409826

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 numberUS08815910B2
Source datasetuspto-grants-2014_08
ORD IDord-25342efa9e834156895d4a53986a58f1
Source noteuspto-grants-2014_08