HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Dimethylaminopyridine → chloro-N-(4-fluoro-3-nitrophenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 4-Fluoro-3-nitroaniline | HCID 67768 | — |
| Reactant | (Chloromethyl)sulfonyl chloride | HCID 77054 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | chloro-N-(4-fluoro-3-nitrophenyl)methanesulfonamide | HCID 18760842 | 93.1% |
Reaction Steps
20 g of 4-fluoro-3-nitroaniline (128 mmol) was dissolved in a mixture of 200 mL of dichloromethane and 40 mL of pyridine. To this solution was added 21 g (140 mmol) of chloromethylsulfonyl chloride dropwise at 20-30° C., followed by the addition of 3.21 g of dimethylaminopyridine. The solution was stirred for an additional 3 hours. The reaction mixture was transferred into a separatory funnel and washed sequentially with water (twice with 25 mL), 5% HCl (twice with 25 mL), and water (25 mL). The organic phase was separated, dried (MgSO4), filtered and concentrated under reduced pressure to yield 32 g (93%) of the title compound as a solid melting at 112-113° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06664400B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-b166d96010af46608c77036a997a1fea |
| Source note | uspto-grants-2003_12 |