HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl isocyanate → N-(Butylaminocarbonyl)-2-chloro-6-phenylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-6-phenylbenzenesulfonamide | HCID 13852352 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(Butylaminocarbonyl)-2-chloro-6-phenylbenzenesulfonamide | HCID 13852353 | 94% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04643761 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-0fe9773b5d3d4222a8064226e90e9782 |
| Source note | uspto-grants-1987_02 |