HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 4-trichloroacetamido-5-hexenoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Trichloroacetonitrile | HCID 11011 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 6-hydroxy-4-hexenoate | HCID 53641333 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 4-trichloroacetamido-5-hexenoate | HCID 11055787 | 727.1% |
Reaction Steps
Sodium hydride (0.03 g of a 50% dispersion in oil, 0.5 mmol, was added to a solution of ethyl 6-hydroxy-4-hexenoate (0.7 g, 5 mmol) and trichloroacetonitrile (0.6 g, 5 mmol) in anhydrous ether (50 mL) under N2 at 0° C. After 1 H, ethanol (0.5 mmol) was added and the solvent was removed in vacuo. The formation of the imidate was controled by NMR (NH,~8.5 ppm). A solution of the crude imidate in xylene (30 mL) was heated at reflux 48 H. Then the solvent was removed in vacuo and the residue was purified by flash chromatography on SiO2. (eluant AcOEt: hexane, 2:8) to give the title product (1.1 g, ~70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05512698 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-d680ef5728934538954b638cdecc0195 |
| Source note | uspto-grants-1996_04 |