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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535319Generated: October 31, 2026

(4-Bromophenyl)(cyclohexyl)methanol → (4-Bromophenyl)(cyclohexyl)methanone

https://huagongshe.com/reaction/535319

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Bromophenyl)(cyclohexyl)methanolHCID 11402947—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product(4-Bromophenyl)(cyclohexyl)methanoneHCID 24261645—

Reaction Steps

To a solution of (4-bromophenyl)(cyclohexyl)methanol (3.45 g, 12.82 mmol) in DCM (100 ml) was added manganese dioxide (11.14 g, 128 mmol) at room temperature. The reaction mixture was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate and the organic phase was washed with aqueous NaHCO3 solution and brine. The organic phase was dried over Na2SO4, filtered and concentrated in vacuo to obtain the title compound as slightly orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859535B2
Source datasetuspto-grants-2014_10
ORD IDord-279e421d6ef94f209b79a09dccf00dc1
Source noteuspto-grants-2014_10