Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601113Generated: October 28, 2026

4-Fluorobenzenesulfonyl chloride → HCID 21697167, compound

https://huagongshe.com/reaction/1601113

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
Reactant3182-88-5HCID 85780938—
SolventHydrochloric AcidHCID 313—
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 numberUS05977141
Source datasetuspto-grants-1999_11
ORD IDord-300bcc7737d542be853cfaf64ed7518e
Source noteuspto-grants-1999_11