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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354236Generated: October 31, 2026

4-Methoxybenzaldehyde → Cyclohexyl-(4-methoxyphenyl)methanol

https://huagongshe.com/reaction/354236

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantHCID 178419651HCID 178419651—
ProductCyclohexyl-(4-methoxyphenyl)methanolHCID 9920862—

Reaction Steps

Referring now to FIG. 2, this alternative synthesis starts from 4-methoxy-benzaldehyde (VI) which is subjected to treatment with cyclohexyl magnesium bromide to yield cyclohexyl-(4-methoxy-phenyl)-methanol (V). This in turn is then oxidised so as to yield cyclohexyl-(4-methoxy-phenyl)-methanone (III).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756502B2
Source datasetuspto-grants-2004_06
ORD IDord-aacd95c11a9f4f8eb70c139deb24342e
Source noteuspto-grants-2004_06