HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995633Generated: October 25, 2026
Hydrochloric Acid → 4-CHLORO-gamma-(1-OXOETHYL)-beta-METHYLBENZENEBUTANENITRILE
https://huagongshe.com/reaction/1995633
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-(p-Chlorophenyl)acetone | HCID 79699 | — |
| Reactant | Crotononitrile | HCID 637921 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4-CHLORO-gamma-(1-OXOETHYL)-beta-METHYLBENZENEBUTANENITRILE | HCID 13502869 | — |
Reaction Steps
Triton B (5.85 ml) was added dropwise to 4-chlorophenylacetone (21.8 grams) in 78 ml of tert. butanol. Next crotononitrile (9.17 grams) was likewise added with initial cooling to lower the temperature to about 20° C. Since the reaction was not exothermic, no additional cooling was necessary after the desired temperature was reached. The reaction was then heated to 65° C. for 21/2 hours and, after chilling in an ice bath, 262 ml of 1 N HCl was added in portions. Next the reaction mixture was extracted with ether, washed with water, dried, and evaporated in vacuo. An oil resulted which was distilled under vacuum, yield 18.6 grams, b.p. 130°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04405552 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-0dd21bb665bc45c1968f04407990635b |
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| Source note | uspto-grants-1983_09 |
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