HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 3-Fluoro-4-methylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3-Fluoro-4-methylbenzene-1-sulfonyl chloride | HCID 2778600 | — |
| Product | 3-Fluoro-4-methylbenzenesulfonamide | HCID 2064138 | — |
Reaction Steps
To ˜20 mL of liquid ammonia at −78° C. was added 2.1 g (10 mmol) of 3-fluoro-4-methyl benzenesulfonyl chloride. The excess ammonia was then naturally evaporated to dryness overnight at room temperature. The crude sulfonamide was partitioned methylene chloride (100 mL) and water (100 mL). The aqueous phase was further extracted with methylene chloride. The combined organic extracts were dried over anhydrous sodium sulfate. Evaporation of the solvents afforded 1.9 g of 3-fluoro-4-methylbenzenesulfonamide as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645771B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-b6eb31ab78bd44929e99e26a1573795f |
| Source note | uspto-grants-2010_01 |