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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900212Generated: October 29, 2026

Iodoacetic Acid → 2-benzoylsulfanylacetic Acid

https://huagongshe.com/reaction/1900212

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 numberUS05574140
Source datasetuspto-grants-1996_11
ORD IDord-6ffaf6a343fb408398eb21be0dd3cf84
Source noteuspto-grants-1996_11