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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22272Erstellt: 24. Oktober 2026

Thioglycolic Acid → HCID 178526169, Verbindung

https://huagongshe.com/de/reaction/22272

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThioglycolic AcidHCID 1133—
EduktPotassium HydroxideHCID 14797—
Edukt3-Bromobenzyl bromideHCID 69979—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktHCID 178526169HCID 17852616992%

Reaktionsschritte

To a solution of 3-bromobenzyl bromide (23.75 g, 90 mmol) and thioglycolic acid (11.42 g, 120 mmol) in ethanol (150 mL) was added potassium hydroxide (14.24 g, 250 mmol) in water (50 mL). The reaction was heated at reflux for 3.5 h, cooled and the ethanol was evaporated. The residue was quenched with water (100 mL) and the mixture was extracted with ether (50 mL). The aqueous layer was acidified to pH 1 with concentrated hydrochloric acid, extracted with ethyl acetate (2×100 mL) and the organic phase was dried. Evaporation of the solvent followed by washing of the residue with hexane afforded 3-bromophenylmethylthioacetic acid as a white solid (92%), mp 90°-91° C.: 1H NMR (CDCl3) δ3.10 (s, 2H), 3.82 (s, 2H), 7.20-7.29 (m, 2H), 7.39-7.42 (dd, 1H), 7.52 (d, 1H); IR (KBr) 1706 cm-1 ; Mass spectrum m/z 280 (M+NH4); Anal. calcd. for C9H9O2SBr: C 41.39, H 3.47, S 12.28; Found C 41.43, H 3.49, S 12.10.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05428040
Quelldatensatzuspto-grants-1995_06
ORD IDord-cd69c48598cb494798ccebfd7e04088b
Quellennotizuspto-grants-1995_06