HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-Methyl-N-(2-nitrophenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | N-Methylmethanesulfonamide | HCID 97632 | — |
| Reactant | Potassium methoxide | HCID 23664618 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Methyl-N-(2-nitrophenyl)methanesulfonamide | HCID 13314625 | 74.4% |
Reaction Steps
To 3.2 g of N-methyl methanesulfonamide in 50 ml of dry dimethylformamide is added 1.47 g of potassium methoxide. The mixture is stirred for 15 minutes. 2.8 g of 2-Fluoronitrobenzene is added and the mixture is heated to reflux for two hours. The dimethylformamide is removed on a rotary evaporator. The concentrated reaction mixture is poured into water. The crude product is extracted with CH2Cl2. The crude extracts are dried with MgSO4, filtered and concentrated on a rotary evaporator. The crude product is purified by recrystallization from butyl chloride-ethyl acetate. 3.4 g of product with m.p. 144°-145° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04629496 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-a4b446c5e57f478f8d86eb6a43e10be8 |
| Source note | uspto-grants-1986_12 |