HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 352955, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N-hydroxybenzenecarboximidoyl chloride | HCID 2756315 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 352955 | HCID 352955 | 36.8% |
Reaction Steps
The 9.4 g of recovered benzohydroximoyl chloride was dissolved in 100 ml of anhydrous ether and the solution was cooled to -20°. To the cold solution was rapidly added 12.3 g of triethylamine. To this mixture was slowly added (during 45 minutes) a solution of 6.95 g of methanesulfonyl chloride in 50 ml of anhydrous ether. The mixture was stirred at -30° for 1 hour, then at ambient temperature for about 16 hours. The mixture was filtered and the filtrate was conconcentrated under reduced pressure to give a yellow solid. The solid was recrystallized from a benzene-hexane mixture to give 5.2 g of N-(methanesulfonyloxy)benzimidoyl chloride, m.p. 106°-108°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983246 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-d652e83444654308bede2657cf553512 |
| Source note | uspto-grants-1976_09 |