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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22415Generated: October 26, 2026

Phenethylamine → 4-((2-Phenylethyl)aminocarbonyl)benzenesulfonamide

https://huagongshe.com/reaction/22415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethylamineHCID 1001—
ReactantTriethylamineHCID 8471—
ReactantCarzenideHCID 8739—
ReactantEthyl chloroformateHCID 10928—
SolventTetrahydrofuranHCID 8028—
Product4-((2-Phenylethyl)aminocarbonyl)benzenesulfonamideHCID 1997074867%

Reaction Conditions

Temperature-10 °C

Reaction Steps

20.1 g (0.1 mol) of 4-carboxy-benzenesulfonamide were suspended in 300 ml of anhydrous tetrahydrofuran, and 15.2 ml (0.11 mol) of triethylamine were added dropwise at 0° C., while stirring. After 30 minutes, 10.5 ml (0.11 mol) of ethyl chloroformate were added dropwise at 0° C., the mixture was stirred at this temperature for 1 hour and cooled to -10° C., and 12.1 g (0.1 mol, 12.5 ml) of 2-phenylethylamine in 30 ml of anhydrous tetrahydrofuran were added dropwise. After 1 hour at 0° C., the mixture was warmed to 20° C. and concentrated in vacuo and the solid residue was treated with water, filtered off with suction and recrystallized from ethanol to give 20.4 g of product, melting point 243° to 245° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428046
Source datasetuspto-grants-1995_06
ORD IDord-350c9a4b7662438bb680d09920db4e0a
Source noteuspto-grants-1995_06