HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → HCID 54542349, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 3303868 | HCID 3303868 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 54542349 | HCID 54542349 | 62.1% |
Reaction Steps
In a second synthesis, 10 g of 4-methylbenzohydroximoyl chloride, 6.7 g of methanesulfonyl chloride, and 160 ml of benzene were mixed in a 250-ml, three-necked, round-bottomed flask equipped with a stirrer, thermometer, and drying tube. Triethylamine (8.8 g) was added dropwise during 6 minutes at 5°-10°, and the mixture was stirred at that temperature for 1 hour. The reaction mixture was filtered, the solid was washed with benzene, the washes and filtrate were combined and concentrated, and the concentrate was recrystallized from ethanol to give 9 g of N-(methanesulfonyloxy)-4-methylbenzimidoyl chloride, m.p. 100°-102°. The ir spectrum was consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983246 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-44cf84dc2d594cc39b56c1b42bd0fd1e |
| Source note | uspto-grants-1976_09 |