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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406060Generated: November 1, 2026

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

https://huagongshe.com/reaction/2406060

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, 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 numberUS08809339B2
Source datasetuspto-grants-2014_08
ORD IDord-c313e60159924ce4a6332de878e7ca8c
Source noteuspto-grants-2014_08