HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653356Generated: October 30, 2026
Diethylene Glycol → HCID 178444309, compound
https://huagongshe.com/reaction/653356
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylene Glycol | HCID 8117 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 178444337 | HCID 178444337 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178444309 | HCID 178444309 | 83% |
Reaction Steps
A mixture of 235 mg of p-[trans-4-(trans-1-pentenyl)cyclohexyl]propiophenone (prepared according to Example 1), 0.161 ml of hydrazine hydrate, 5 ml of diethylene glycol and 5 ml of ethanol was heated to reflux for 30 minutes under an argon atmosphere in a round flask provided with a reflux condenser. The mixture was then treated with 195 mg of solid potassium hydroxide and subsequently gradually heated to 200° C., while distilling off the ethanol, and held at this temperature for 2 hours. The cooled mixture was poured into 50 ml of water and extracted three times with 50 ml of petroleum ether each time. The organic phases were washed three times with 50 ml of water each time, dried over magnesium sulphate and concentrated. Low-pressure chromatography (0.5 bar) of the residue with hexane on a short column of silica gel gave 185 mg (83%) of 4-propyl-1-[trans-4-(trans-1-pentenyl)cyclohexyl]benzene as a colourless liquid; purity 98.6%, m.p. (C--I) 7.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04676604 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-5d6d677a2b034b33bbc23cf156b80b53 |
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| Source note | uspto-grants-1987_06 |
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