HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → ethyl 3-(2-propylidenehydrazinyl)-2-(2,3,4,5-tetrafluorobenzoyl)prop-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Reactant | Ethyl 3-ethoxy-2-(2,3,4,5-tetrafluorobenzoyl)acrylate | HCID 54346083 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 3-(2-propylidenehydrazinyl)-2-(2,3,4,5-tetrafluorobenzoyl)prop-2-enoate | HCID 178458059 | 72.2% |
Reaction Steps
First 2.8 g of hydrazine hydrate and, 30 minutes later, 12.8 g of acetone are added dropwise to a solution of 16 g of ethyl 2-(2,3,4,5-tetrafluorobenzoyl)-3-ethoxyacrylate in 70 ml of ethanol, while cooling with dry ice/acetone at -25° C. to -30° C. The mixture is allowed to come slowly to room temperature and is then stirred at 20° C. to 25° C. for a further hour. The solvent is then distilled off in vacuo and the orange-colored residue is recrystallized from cyclohexane/light petrol. 12.5 g of ethyl 2-(2,3,4,5-tetrafluorobenzoyl)-3-(2-propylidenehydrazino)acrylate of melting point 86° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04753925 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-dba5329a6b904844a502102faee4bde5 |
| Source note | uspto-grants-1988_06 |