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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464849Generated: October 30, 2026

Ethanol → (4-(3-Propylcyclopentyl)cyclohexyl)methanol

https://huagongshe.com/reaction/1464849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(3-Propylcyclopentyl)cyclohexanecarboaldehydeHCID 86660291—
SolventWaterHCID 962—
Product(4-(3-Propylcyclopentyl)cyclohexyl)methanolHCID 6799236190.5%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999197B2
Source datasetuspto-grants-2015_04
ORD IDord-19c8f0e582fd4540b00dc927abea3db4
Source noteuspto-grants-2015_04