HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464849Generated: October 30, 2026
Ethanol → (4-(3-Propylcyclopentyl)cyclohexyl)methanol
https://huagongshe.com/reaction/1464849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(3-Propylcyclopentyl)cyclohexanecarboaldehyde | HCID 86660291 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-(3-Propylcyclopentyl)cyclohexyl)methanol | HCID 67992361 | 90.5% |
Reaction Steps
Ethanol (30 ml) was added to 4-(3-propylcyclopentyl)cyclohexanecarboaldehyde (2.3 g) obtained in the second step in Example 3, in a reaction vessel under an atmosphere of nitrogen, and the mixture was cooled to 0° C., and sodium borohydride (0.22 g) was added slowly. After the mixture had been returned to room temperature and stirred for another 20 hours and water (30 ml) was added. The mixture was separated, and the water layer was extracted with diethyl ether three times, and then the combined organic layer was washed with brine. The solution was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane=1/2 by volume) to give (4-(3-propylcyclopentyl)cyclohexyl)methanol (2.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999197B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-19c8f0e582fd4540b00dc927abea3db4 |
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| Source note | uspto-grants-2015_04 |
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