HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 4-ethoxycarbonimidoyl-4-(2-trifluoromethylphenyl)butanoate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Methyl 4-cyano-4-(2-trifluoromethylphenyl)butanoate | HCID 66618793 | — |
| Product | Ethyl 4-ethoxycarbonimidoyl-4-(2-trifluoromethylphenyl)butanoate hydrochloride | HCID 66628906 | — |
Reaction Steps
Methyl 4-cyano-4-(2-trifluoromethylphenyl)butanoate (200 mg) was dissolved in ethanol (1.03 mL), and acetyl chloride (838 μl) was added at 0° C. The mixture was heated to room temperature and the reaction was initiated. After stirring for 24 hours, concentration under reduced pressure gave a crude product of the title compound as an oil (300 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754100B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-2c988077b71f41e39b000cb2a63e958e |
| Source note | uspto-grants-2014_06 |