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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378931Generated: October 30, 2026

Hydrochloric Acid → HCID 21697167, compound

https://huagongshe.com/reaction/378931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
Reactant3182-88-5HCID 85780938—
SolventWaterHCID 962—
ProductHCID 21697167HCID 21697167—

Reaction Steps

A mixture of isobutylamino-acetic acid, ethyl ester hydrochloride (0.359 g, 0.00183 mol) in. 6 M hydrochloric acid (10 mL) was refluxed for 20 hours and allowed to cool. The mixture was made basic with 50% wt/wt sodium hydroxide and 1 M sodium hydroxide to pH=5, and the volatiles were rotary evaporated. The residue was triturated 3 times with boiling methanol, and the triturates were combined and rotary evaporated. The residue was triturated 3 times with hot acetic acid, and the triturates were combined and rotary evaporated. The residue was dissolved in water and freeze-dried to give a white solid. This solid was combined with 4-fluoro-benzenesulfonyl chloride (0.3334 g, 0.001713 mol) and sodium carbonate (0.547 g, 0.00516 mol) in water, and the mixture was stirred at room temperature for 3 days. The mixture was acidified with concentrated hydrochloric acid and extracted with ethyl acetate. The extract was dried (MgSO4) and rotary evaporated to a white solid. The solid was chromatographed on silica gel (15 g, 230-400 mesh) eluting with dichloromethane-methanol (10:1, 10×15 mL). Fractions containing product were combined and rotary evaporated to give a white solid. The solid was dried in vacuo; yield 0.32 g (64% overall).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297247B1
Source datasetuspto-grants-2001_10
ORD IDord-6f831d205cae4cf8b7cf5341fee23bc3
Source noteuspto-grants-2001_10