HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → N-(2-acetoacetoxyethyl)N-cyclohexyl-4-(6-carbostyriloxy)butyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diketene | HCID 12661 | — |
| Reactant | N-cyclohexyl-N-(2-hydroxyethyl)-4-(6-carbostyriloxy)butyramide | HCID 12866343 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-(2-acetoacetoxyethyl)N-cyclohexyl-4-(6-carbostyriloxy)butyramide | HCID 20250808 | 69.3% |
Reaction Steps
To 100 ml of dimethylformamide, there were added 7.45 g of N-cyclohexyl-N-(2-hydroxyethyl)-4-(6-carbostyriloxy)butyramide and 0.5 ml of triethylamine, then the whole mixture was heated at 80° to 90° C. on an oil bath. Next, 1.8 g of diketene were added dropwise to the reaction mixture, then the mixture was stirred for 1 hour at the same temperature. The reaction mixture was concentrated then was purified by a silica gel column chromatography (eluant: chloroform/methanol=50/1), and the solvent was removed by distillation under reduced pressure to yield 6.33 g of N-(2-acetoacetoxyethyl)N-cyclohexyl-4-(6-carbostyriloxy)butyramide in the form of a brownish oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04564619 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-e85660938ee24dbd953de6b47dce7012 |
| Source note | uspto-grants-1986_01 |