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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 905181Erstellt: 25. Oktober 2026

Hydrochloric Acid → (4R)-3-(S-Benzoyl-3-mercaptopropanoyl)-2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acid

https://huagongshe.com/reaction/905181

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt(4R)-2-(2-hydroxyphenyl)-1,3-thiazolidine-4-carboxylic acidHCID 2825745—
EduktHCID 13013918HCID 13013918—
LösungsmittelAcetoneHCID 180—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(4R)-3-(S-Benzoyl-3-mercaptopropanoyl)-2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acidHCID 12915688—

Reaktionsschritte

11.3 g of (4R)-2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acid and 13.2 g of thriethylamine are dissolved in 200 ml of dehydrated acetone and 11.7 g of S-benzoyl-3-mercaptopropanoyl chloride is added dropwise while stirring under ice-cooling. After the addition, the mixture is stirred under ice-cooling for 1 hour. 4 N Hydrochloric acid in ether is added to this mixture and the precipitate is filtered. The filtrate is concentrated in vacuo and the obtained oil is dissolved in ethyl acetate, washed with 2 N hydrochloric acid and saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated to dryness in vacuo to give the titled compound, yield 12 g (58%), mp. 100.5°-101° C. (dec.) (ethyl acetatebenzene), [α]D26 +130.8° (c=1.0, methanol).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04423054
Quelldatensatzuspto-grants-1983_12
ORD IDord-b673c358e9594080bd4010f2d8e94693
Quellennotizuspto-grants-1983_12