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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560117Generated: October 25, 2026

Benzenesulfonyl chloride → 2-{benzenesulfonyl-[2-(3-bromo-phenyl)-2-hydroxy-ethyl]-amino}-N-phenyl-acetamide

https://huagongshe.com/reaction/560117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantDiisopropylethylamineHCID 81531—
ReactantPotassium bisulfateHCID 516920—
Reactant2-[2-(3-bromo-phenyl)-2-hydroxy-ethylamino]-N-phenyl-acetamideHCID 67000657—
SolventDichloromethaneHCID 6344—
Product2-{benzenesulfonyl-[2-(3-bromo-phenyl)-2-hydroxy-ethyl]-amino}-N-phenyl-acetamideHCID 6700109099%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled suspension of 2-[2-(3-bromo-phenyl)-2-hydroxy-ethylamino]-N-phenyl-acetamide (840 mg) and N,N-diisopropylethylamine (760 mL) in methylene chloride (20 mL) was added benzenesulfonyl chloride (0.31 mL). The mixture was stirred at 0° C. for 1 hour and at room temperature overnight. A 1M aqueous solution of KHSO4 was added, the phases were separated, and the inorganic one was extracted with ethyl acetate (×2). The combined organic layers were washed with brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, n-heptanelethyl acetate 1:1) to yield 2-{benzenesulfonyl-[2-(3-bromo-phenyl)-2-hydroxy-ethyl]-amino}-N-phenyl-acetamide (1.17 g, 99%) as a white foam, MS: 489.0 (M+H, 1Br)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063088B2
Source datasetuspto-grants-2011_11
ORD IDord-a8fa243c783a4b308a853d399fde4904
Source noteuspto-grants-2011_11