HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21543983, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isoxazolium, 2-(1,1-dimethylethyl)-5-methyl-, perchlorate (1:1) | HCID 151520 | — |
| Reactant | HCID 21543990 | HCID 21543990 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21543983 | HCID 21543983 | — |
Reaction Steps
N-tert-butyl-5-methylisoxazolium perchlorate (120 g.; 0.005 mole) is added to a solution of 2-furfurylamino-4-chloro-5-methylsulfonylbenzoic acid (1.65 g.; 0.005 mole) and triethylamine (0.7 ml.) in dimethylformamide (15 ml.). The resulting solution is allowed to stir at room temperature for 2 hours, and then diluted with H2O (75 ml.). The white solid which precipitates is collected and dried, yield 2.4 g. (crude), m.p. 140°-145° C. Recrystallization from butyl chloride yields N-tert-butyl-3-(2-furfurylamino-4-chloro-5-methylsulfonylbenzoyloxy)crotonamide, m.p. 148.5°-150° C. (dec. with eff.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03953476 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-8786dac8b5f542c69a25bea4a301318c |
| Source note | uspto-grants-1976_04 |