HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → N-methyl-1-(3-nitrophenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | (3-Nitrophenyl)methanesulfonyl chloride | HCID 13196775 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-methyl-1-(3-nitrophenyl)methanesulfonamide | HCID 13286046 | 87.7% |
Reaction Steps
40% aqueous methylamine (10 mL, 0.1 mol) was added to a vigorously stirred solution of (3-Nitrophenyl)methanesulfonyl chloride (1.18 g, 5 mmol) in benzene (30 mL) and allowed to stir for 2 h at room temperature. To this end, the benzene layer was separated, and the aqueous layer extracted with CH2Cl2 (2×25 mL). The combined organic layers were washed with saturated aqueous NaHCO3 (30 mL), water (30 mL), filtered over anhydrous Na2SO4, filtered and the solvent removed under reduced pressure to give 1.01 g (87%) of (3-nitrophenyl)-N-methylmethanesulfonamide as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507498B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-a2ef2018ab324f2482fe20ffa3f88998 |
| Source note | uspto-grants-2013_08 |