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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342335Generated: October 25, 2026

Iodoacetic Acid → 2-benzoylsulfanylacetic Acid

https://huagongshe.com/reaction/342335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoacetic AcidHCID 5240—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178526132HCID 178526132—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-benzoylsulfanylacetic AcidHCID 511653399%

Reaction Steps

To a purged stirring solution at 0° C. of (5.74 g, 41.6 mmoles) thiobenzoic acid in (100 mL) ethanol was added (27.8 mL, 3N, 83.2 mmoles) potassium hydroxide followed by (7.70 g, 41.6 mmoles) iodoacetic acid in (30 mL) ethanol. The solution stirred for 10 hours at room temperature under argon. The ethanol was rotavapped and the orange solid product was dissolved in (40 mL) water. The solution was acidified to pH 2.0 where an orange precipitate formed. This was filtered, washed with water, and dried in vacuo to give (7.98 g, 99% yield) benzoylmercaptoacetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05858327
Source datasetuspto-grants-1999_01
ORD IDord-ab83a9594a4143f8a4a69464d3ec7286
Source noteuspto-grants-1999_01