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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566853Generated: October 26, 2026

4,6,6-Trimethyl-1,3-cyclohexadiene-1-carboxaldehyde → 4,6,6-Trimethyl-1,3-cyclohexadiene-1-methanol

https://huagongshe.com/reaction/566853

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6,6-Trimethyl-1,3-cyclohexadiene-1-carboxaldehydeHCID 10920683—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product4,6,6-Trimethyl-1,3-cyclohexadiene-1-methanolHCID 2126374356%

Reaction Steps

A solution of 20 g (133 mole) of 4,6,6-trimethyl-1,3-cyclohexadiene-1-carbaldehyde in 100 ml of diethylether was added to a suspension of 1.5 g (39 mmole) of LiAlH4 in diethylether, under stirring and cooling with an ice-bath. After 1 h of reaction time, the mixture was hydrolyzed, the organic layer was separated, washed and dried and concentrated. The crude product was then distilled in vacuo, b.p. 60°/20 hPa, to obtain 11.6 g (56%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177400B1
Source datasetuspto-grants-2001_01
ORD IDord-5ac3980826f6428d87d831b586e1b8ca
Source noteuspto-grants-2001_01