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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236231Generated: October 29, 2026

Butyl isocyanate → N-(Butylaminocarbonyl)-2-chloro-6-phenylbenzenesulfonamide

https://huagongshe.com/reaction/236231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl isocyanateHCID 8110—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-6-phenylbenzenesulfonamideHCID 13852352—
SolventAcetonitrileHCID 6342—
ProductN-(Butylaminocarbonyl)-2-chloro-6-phenylbenzenesulfonamideHCID 1385235394%

Reaction Steps

A mixture of 7.7 g (0.029 mol) 2-chloro-6-phenylbenzenesulfonamide, 3.6 ml (0.032 mol) n-butylisocyanate and 4.1 g (0.03 mol) potassium carbonate was heated in 80 ml dry acetonitrile for 18 hours at reflux. The solvent was evaporated and the residue treated with 1N HCl and ethyl acetate and the insoluble solids were collected, washed with water and then ether. Additional material was obtained from the organic phase of the filtrate to afford a total of 10 g of the title compound, m.p. 184°-186°. NMR (90 MHz, CDCl3), 0.9 (CH3, t, br), 1.4 (4H, m), 3.05 (q, J=7 Hz, 2H), 5.9 (t, br, NH), 7.2-7.6 (m, 8H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04643761
Source datasetuspto-grants-1987_02
ORD IDord-0fe9773b5d3d4222a8064226e90e9782
Source noteuspto-grants-1987_02