HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-(2-Benzoyl-4-chlorophenyl)prop-2-enenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 3-(2-Benzyl-4-chlorophenyl)prop-2-enenitrile | HCID 54560380 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(2-Benzoyl-4-chlorophenyl)prop-2-enenitrile | HCID 54314020 | — |
Reaction Steps
A mixture of 28.8 g (0.14 mol) of 3-[2-benzyl-4-chlorophenyl]-2-propenenitrile, 50 g (0.5 mol) of chromium trioxide, 100 ml of methylene chloride, and 300 ml of acetic acid was stirred at room temperature overnight. The excess chromium trioxide was discharged by the slow addition of 30 ml of ethanol. The mixture was diluted with 800 ml of water and extracted with 500 ml of ether. The ether solution was washed with water, saturated aqueous sodium bicarbonate, and saturated aqueous sodium chloride. The ether solution was dried over anhydrous sodium sulfate and concentrated at reduced pressure to give a yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04436662 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-26938e1d16094e70873d8b1f70baa312 |
| Source note | uspto-grants-1984_03 |