HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 3-Fluoro-4-nitrobenzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-Fluoro-4-nitrobenzenesulfonyl chloride | HCID 15569555 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Fluoro-4-nitrobenzene-1-sulfonamide | HCID 58158695 | 99% |
Reaction Steps
To a solution of 5.00 g 3-fluoro-4-nitrobenzenesulfonyl chloride in 20 mL acetonitrile cooled in an ice bath was added dropwise 4.40 mL of a 30% ammonium hydroxide solution. After removal of the ice bath, stirring was continued for 30 min. at room temperature. Water was added and the mixture was extracted with DCM. The combined organic layers were dried over MgSO4 and evaporated to dryness to give 4.65 g (99%) of a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 7.51 (s, 2H), 7.89 (d, J=9.33 Hz, 1H), 7.92 (dd, J=10.23, 1.81 Hz, 1H), 8.14-8.21 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08563723B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-99e96d905de34635b74e1f05eef64e99 |
| Source note | uspto-grants-2013_10 |