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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434764Generated: October 30, 2026

2-Isopropylcyclohexan-1-ol → 2-Isopropylcyclohexan-1-one

https://huagongshe.com/reaction/434764

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Isopropylcyclohexan-1-olHCID 95331—
ReactantHCID 178526115HCID 178526115—
SolventDichloromethaneHCID 6344—
Product2-Isopropylcyclohexan-1-oneHCID 70490—

Reaction Steps

To a suspension of 4.0 g. (13.7 mmole) of 2,2'-bipyridinium chlorochromate in 15 ml of dichloromethane is added, while stirring, 0.5 g. (3.5 mmole) of 2-isopropylcyclohexanol in 10 ml of dichloromethane. The resulting reaction mixture is stirred for 4 hours and then filtered through a Hirsch funnel packed with 2 cm of Celite®. The resulting clear filtrate is washed with 5% hydrochloric acid and 10% sodium carbonate, and dried over magnesium sulfate. The drying agent is then removed and the solvent evaporated to yield a colorless oil which is distilled via Kugelrohr to yield pure 2-isopropylcyclohexanone in a typical yield of 0.425 g. which is 86% of theoretical yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399281
Source datasetuspto-grants-1983_08
ORD IDord-202a73537e6b474f91ffe9d816766776
Source noteuspto-grants-1983_08