HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223477Generated: October 30, 2026
Diethyl Ether → alpha,4-Dichloro-2-(benzoyl)benzenepropanenitrile
https://huagongshe.com/reaction/223477
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | 2-Amino-5-chlorobenzophenone | HCID 12870 | — |
| Reactant | 2,5-Dichlorobenzophenone | HCID 458188 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | alpha,4-Dichloro-2-(benzoyl)benzenepropanenitrile | HCID 13067144 | — |
Reaction Steps
A solution of 92.7 g (0.4 mole) of 2-amino-5-chlorobenzophenone in 250 ml of acetonitrile was added to a mixture of 70 g (0.52 mole) of cupric chloride, 65 g (0.63 mole) of t-butylnitrile, 500 ml of acrylonitrile, and 500 ml of acetonitrile. When the addition was complete stirring at room temperature was continued for 2 hr. The mixture was diluted with 80 ml of 6 N hydrochloric acid and 1500 ml of water, extracted with ether and dried over anhydrous sodium sulfate. The ether solution was concentrated at reduced pressure to give a bronw oil, which contained the end product and 2,5-dichlorobenzophenone. Trituration of the oil with a mixture of ether and petroleum ether gave the end product as a tan solid. Recrystallization of a small portion of the end product from a mixture of ether and petroleum ether gave pale yellow needles, mp 69°-71°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04354973 |
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| Source dataset | uspto-grants-1982_10 |
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| ORD ID | ord-b45e0d809e754931bddb5cfab5ca4c23 |
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| Source note | uspto-grants-1982_10 |
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