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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 342333Erstellt: 25. Oktober 2026

Iodoacetic Acid → 2-benzoylsulfanylacetic Acid

https://huagongshe.com/reaction/342333

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodoacetic AcidHCID 5240—
EduktPotassium HydroxideHCID 14797—
EduktHCID 178526132HCID 178526132—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt2-benzoylsulfanylacetic AcidHCID 511653399%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05858327
Quelldatensatzuspto-grants-1999_01
ORD IDord-bc621f3a94e34b4eb43a698b88d1236a
Quellennotizuspto-grants-1999_01