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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398273Generated: October 25, 2026

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

https://huagongshe.com/reaction/398273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantN-(4-Hydroxyphenyl)glycineHCID 67149—
Reactant5-Chlorothiophene-2-sulfonyl chlorideHCID 2733925—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventSodium HydroxideHCID 14798—
Product5-Chloro-N-[(S)-2-hydroxy-1-(4-hydroxycyclohexyl)ethyl]thiophene-2-sulfonamideHCID 59086185—

Reaction Conditions

Temperature0 °C

Reaction Steps

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)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610734B2
Source datasetuspto-grants-2003_08
ORD IDord-14d8f51c5c6e4961864a90bb7cf32a45
Source noteuspto-grants-2003_08