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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327687Generated: November 3, 2026

Triethylamine → Sulfamic acid 4-oxo-4-phenylbutyl ester

https://huagongshe.com/reaction/327687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorosulfamic acidHCID 24499—
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant4-Hydroxy-1-phenylbutan-1-oneHCID 10975816—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductSulfamic acid 4-oxo-4-phenylbutyl esterHCID 5417745340.1%

Reaction Steps

A cold (-10° C.) solution of 5.20 ml (0.06 mole) chlorosulfonyl isocyanate in 50 ml of methylene chloride was treated with a solution of 0.11 ml of water in 5 ml of acetonitrile over a period of 30 min. A solution of 6.56 g (0.04 mole) of 4-oxo-4-phenylbutanol and 8.34 ml (0.06 mole) of triethylamine in 30 ml of methylene chloride was then added to the solution of the sulfamoyl chloride at 0° to 10° C. over 20 min. The reaction mixture was stirred at room temperature for 4 hr. extracted once with water and once with sodium bicarbonate solution. The aqueous layers were back extracted with methylene chloride. The combined organic layers were dried (magnesium sulfate) and concentrated to an oil that solidified on standing. The solid was triturated with 1,1,1-trichloroethane to give 3.90 g of off-white solid. Recrystallization from acetonitrile-1,1,1-trichlorethane yielded 3.2 g of off-white solid, mp 78°-80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273993
Source datasetuspto-grants-1993_12
ORD IDord-b645d68d8b9b487d931f8b626348d6b1
Source noteuspto-grants-1993_12