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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729068Generated: October 23, 2026

(1-Phenylcyclopentyl)methanol → 1-Phenylcyclohexanemethanol

https://huagongshe.com/en/reaction/1729068

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-Phenylcyclopentyl)methanolHCID 123544—
ReactantMethyl 1-phenylcyclohexane-1-carboxylateHCID 15105202—
ReactantAluminium lithium hydrideHCID 21226445—
Product1-PhenylcyclohexanemethanolHCID 198517—

Reaction Steps

This compound was prepared (1.02 g, 5.43 mmol, 62%) from the product of Step B (1.91 g, 8.76 mmol) using LiAlH4 (0.75 g, 37.95 mmol) according to the procedure for synthesizing 1-phenylcyclopentanemethanol set forth in Step B, Example 1, with the exception that this compound precipitated out of solution following the steps of: (a) destroying the excess hydride; (b) separating the aluminum salts by filtration; and (c) washing with water (3×4 mL in this Example). Filtration of the precipitate gave 1-phenylcyclohexanemethanol as a white solid, mp 63°-64° C. (compared with reported value, J. Org. Chem. 27:3434 (1962), of 63°-64° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05331010
Source datasetuspto-grants-1994_07
ORD IDord-0fd12617cab34d8cae6425175de8170b
Source noteuspto-grants-1994_07