HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 4-(N-methylacetamido)benzene-1-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | N-Methylacetanilide | HCID 11364 | — |
| Reactant | HCID 178527254 | HCID 178527254 | — |
| Product | 4-(N-methylacetamido)benzene-1-sulfonyl chloride | HCID 293146 | 11% |
Reaction Steps
A solution of N-methyl-N-phenylacetamide (11 g, 73.83 mmol) in dichloromethane (20 mL) was added dropwise to HSO3Cl (80 g, 689.66 mmol) at 5° C. The resulting solution was then stirred at room temperature overnight. The reaction mixture was then quenched by adding 100 mL of iced water. The resulting solution was extracted using dichloromethane (2×50 mL) and the organic layers were combined. The residue was purified by column chromatography using a 10:1 ethyl acetate/petroleum ether solvent system to give 2.2 g (11%) of 4-(N-methylacetamido)benzene-1-sulfonyl chloride as a white solid. 1H NMR (CDCl3) δ 8.09 (d, 2H), 7.48 (d, 2H), 3.38 (s, 3H), 2.17 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07696229B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-a751b95310f64630b0608d841bec1ac2 |
| Source note | uspto-grants-2010_04 |