HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254984Generated: October 25, 2026
Hydrochloric Acid → HCID 178444555, compound
https://huagongshe.com/reaction/2254984
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethylene Glycol | HCID 8117 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178444522 | HCID 178444522 | — |
| Product | HCID 178444555 | HCID 178444555 | 90% |
Reaction Steps
A solution of 2.9 g of trans-4-(4-pentenyl)cyclohexanecarbonitrile in 80 ml of diethylene glycol was treated with 8.0 g of potassium hydroxide and the mixture was stirred for 3.5 hours at a bath temperature of 180° C. Subsequently, the reaction mixture was treated with ice, made acid with 25 ml of 25 percent hydrochloric acid and partitioned in methylene chloride/water. The aqueous phase was extracted three times with methylene chloride. The organic phases were washed twice with water, dried over magnesium sulphate, filtered and concentrated. Chromatographic separation of the brown, oily residue (3.5 g) on silica gel with ethyl acetate/petroleum ether (vol. 10:90) gave 2.9 g (90%) of trans-4-(4-pentenyl)cyclohexanecarboxylic acid as a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05238602 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-f4d40b076efd488dabe3182071a25828 |
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| Source note | uspto-grants-1993_08 |
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