HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285871Generated: October 31, 2026
Hydrochloric Acid → HCID 178443553, compound
https://huagongshe.com/reaction/2285871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Red-Al | HCID 16684438 | — |
| Reactant | HCID 86736934 | HCID 86736934 | — |
| Reactant | HCID 178443556 | HCID 178443556 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178443553 | HCID 178443553 | — |
| Product | HCID 178443554 | HCID 178443554 | — |
Reaction Steps
Introduce 84 ml (0.3 mole) Vitride reducing agent (e.g. sodium-bis-(2-methoxy-ethoxy)aluminum hydride) and about 250 ml of dry benzene (or toluene) into 3-neck flask fitted with a condenser and air-stirrer and bring to reflux. Add dropwise in a course of 30 minutes a solution of 30 g trans-4(4-heptylcyclohexyl)benzoic acid in benzene and continue to reflux for additional 3-4 hours. Mixture is then cooled to room temperature and introduced slowly with stirring into a 20% aqueous HCl solution plus ice. After addition, the mixture is vigorously stirred for another 20 to 30 minutes and resulting layers are then separated. Evaporation of benzene yielded the desired compound, trans-4-(4-heptylcyclohexyl)benzylalcohol in typically 99.9% purity by gas chromatography and yields over 95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04325830 |
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| Source dataset | uspto-grants-1982_04 |
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| ORD ID | ord-fe6ae1368f8545f09a4609d3479ec064 |
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| Source note | uspto-grants-1982_04 |
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