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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358889Generated: October 31, 2026

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

https://huagongshe.com/reaction/2358889

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=½ by volume) to give (4-(3-propylcyclopentyl)cyclohexyl)methanol (2.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685274B2
Source datasetuspto-grants-2014_04
ORD IDord-a53682817a5d4772b33647ce6ac8464c
Source noteuspto-grants-2014_04