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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347343Generated: October 25, 2026

Hydrochloric Acid → 2-(4-Acetylbenzenesulfonamido)acetic acid

https://huagongshe.com/reaction/347343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantGlycineHCID 750—
Reactant4-Acetylbenzenesulfonyl chlorideHCID 266418—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Product2-(4-Acetylbenzenesulfonamido)acetic acidHCID 212012994%

Reaction Steps

Ex-26A: To a solution of 4-acetylbenzenesulfonyl chloride (0.50 g, 2.3 mmol) in acetone (7.5 mL) was added a solution of glycine (0.42 g, 5.7 mmol) in 5% aqueous sodium hydroxide (2.5 mL) and the reaction was stirred for 30 min at room temperature. The mixture was diluted with water (10 mL), acidified with a 1 N hydrochloric acid solution, and extracted with ethyl acetate (3×15 mL). The combined organic layers were washed with brine (2×20 mL), dried over sodium sulfate, and the solvent was removed under reduced pressure. The resulting solid was dried in vacuo to afford 0.55 g (94%) of (4-acetylbenzenesulfonylamino)acetic acid as a white solid, mp 213–215° C. 1H-NMR (300 MHz, DMSO-d6) δ 8.28 (t, 1H, J=5.4 Hz), 8.12 (d, 2H, J=8.4 Hz), 7.92 (d, 2H, J=8.4 Hz), 3.64 (d, 2H, J=5.1 Hz), 2.64 (s, 3H). Anal. Calcd. for C10H11NO5S: C, 46.69; H, 4.31; N, 5.44; S, 12.46; Found: C, 46.76; H, 4.43; N, 5.39; S, 12.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173129B2
Source datasetuspto-grants-2007_02
ORD IDord-70e74d112109419aa05a8de43b0508bc
Source noteuspto-grants-2007_02