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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 398273Erstellt: 24. Oktober 2026

Water → 5-Chloro-N-[(S)-2-hydroxy-1-(4-hydroxycyclohexyl)ethyl]thiophene-2-sulfonamide

https://huagongshe.com/de/reaction/398273

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
EduktN-(4-Hydroxyphenyl)glycineHCID 67149—
Edukt5-Chlorothiophene-2-sulfonyl chlorideHCID 2733925—
EduktHCID 178418361HCID 178418361—
KatalysatorNickelHCID 935—
LösungsmittelSodium HydroxideHCID 14798—
Produkt5-Chloro-N-[(S)-2-hydroxy-1-(4-hydroxycyclohexyl)ethyl]thiophene-2-sulfonamideHCID 59086185—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 4-hydroxy-L-phenylglycine (10 g, 60 mmole) in NaOH (20 mL, 3M) was added water (380 mL) and Raney nickel (30 g). The reaction mixture was hydrogenated at about 3 atm at 60 to 80° C. for 36 h in a hydrogen bomb. The reaction mixture was filtered through Celite and reduced in volume to about 80-100 mL and dioxane (100 mL) was added. The resulting mixture was cooled to 0° C. and treated with Et3N (10 mL) and 5-chlorothiophene-2-sulfonyl chloride (16 g, 72 mmoles). The reaction was allowed to warm up to 25° C. and stirred overnight. The dioxane and Et3N were removed and the remaining aqueous solution diluted with 1N aq. HCl. The resulting precipitate was collected, washed with water and diethyl ether to give the desired product as a white solid (12 g, 50% in two steps) (100% purity by ELSD, m/z=352 (M−1)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06610734B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-14d8f51c5c6e4961864a90bb7cf32a45
Quellennotizuspto-grants-2003_08