HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-(1-Chloroethyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2-(1-Chloroethyl)benzenesulfonyl chloride | HCID 13364625 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(1-Chloroethyl)benzenesulfonamide | HCID 13364628 | — |
Reaction Steps
A solution of ammonia (1.2 ml) in tetrahydrofuran (100 ml) at -70° was contacted rapidly with a solution of 2-(1-chloroethyl)benzenesulfonyl chloride (4.32 g, 18.1 mmol) in tetrahydrofuran (50 ml). The stirred mixture was allowed to warm to 0° and volatiles were removed under reduced pressure. The residue was taken up in ethyl acetate and washed with a small volume of water and brine. The dried (MgSO4) solution was evaporated to give 4.7 g of off white solid which was recrystallized from chloroform to give 3.13 g, m.p. 121°-122°. 1H nmr δ(CD3)2COTMS 8.25-7.30 (m), 6.93 (brds), 6.25 (q, J=7 Hz), 3.17 (s), 1.98 (d, J=7 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04723990 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-81369e951b824169a8227c813fb01c19 |
| Source note | uspto-grants-1988_02 |