Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837420Generated: November 4, 2026

Formaldehyde → 6-Methyl-3-cyclohexene-1,1-dimethanol

https://huagongshe.com/reaction/1837420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant1,3-ButadieneHCID 7845—
ReactantPotassium HydroxideHCID 14797—
Reactant6-Methyl-3-cyclohexene-1-carboxaldehydeHCID 101550—
ReactantCrotonaldehydeHCID 447466—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product6-Methyl-3-cyclohexene-1,1-dimethanolHCID 13899782%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a three-necked flask, 327 g of 2-methyl-4-cyclohexene-1-carboaldehyde, a Diels-Alder reaction product of butadiene and crotonaldehyde, 600 ml of methanol and 729 g of 37% of formalin were charged, and then the temperature of this solution was raised to 60° C. with stirring. Next, 252 g of KOH dissolved in 600 ml of distilled water was added dropwise thereto. After stirring for 7 hours, the reaction solution was concentrated under reduced pressure, which resulted in a residue with two phases. The oil phase concentrated to about 150 ml was washed with 300 ml of distilled water. After concentration under reduced pressure, 50 mg of 3,5-di(t-butyl)-4-hydroxytoluene (BHT) was added to the oil phase, and then vacuum distillation was carried out to yield 311 g (yield 82%) of 6-methyl-3-cyclohexene-1,1-dimethanol as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06783840B2
Source datasetuspto-grants-2004_08
ORD IDord-e38855075db9499d8eb7bccfe03858b1
Source noteuspto-grants-2004_08