HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169287Generated: November 2, 2026
Hydrochloric Acid → 1-Phenylcyclohexanecarbonitrile
https://huagongshe.com/reaction/2169287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ether dimethylsulfoxide | HCID 19869614 | — |
| Product | 1-Phenylcyclohexanecarbonitrile | HCID 75148 | 65.8% |
Reaction Steps
To a suspension of NaH (42.7 g, 1067.0 mmol, 60%) in dimethyl sulfoxide (600.0 mL) were added drop-wise a mixture of phenylacetonitrile (50.0 g, 426.8 mmol) and 1,5-dibromopentane (58.1 mL, 426.8 mmol) dissolved in dimethyl sulfoxide:ether (1:1) (200.0 mL) at 0° C. and the reaction mixture was stirred at this temperature for 2 h. After completion of the reaction, water and a 10% HCl solution were added to the mixture and the mixture was extracted with ethyl acetate. The combined organic layer was then washed with water and brine and dried over sodium sulfate and concentrated under reduced pressure to obtain a crude product. This crude product was then purified by normal silica gel column chromatography (using hexane) to get 1-phenyl-cyclohexanecarbonitrile (249) (52.0 g, 65.76%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045486B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-60fd92c382fa47ff86af1ae4cef1a4db |
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| Source note | uspto-grants-2015_06 |
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