HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Nitrobenzenesulfonyl chloride → N-(Benzyloxy)-2-nitrobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| Reactant | O-Benzylhydroxylamine | HCID 102313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(Benzyloxy)-2-nitrobenzenesulfonamide | HCID 9839578 | 93.2% |
Reaction Steps
A solution of 96.4 g of O-benzylhydroxylamine in 80 ml of tetrahydrofuran was added to a solution of 86.8 g of o-nitrobenzenesulfonyl chloride in 400 ml of tetrahydrofuran at 5°-10°. After stirring at ambient temperature for 16 hours the solvent was evaporated. The residue was washed with water, filtered and dried to give 112.6 g of N-(phenylmethoxy)-2-nitrobenzenesulfonamide, m.p. 148°-151°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04417917 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-0eb95f8257334817bf38805635a23b9f |
| Source note | uspto-grants-1983_11 |