Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395218Generated: November 1, 2026

2-Methyl-3-[4-(2-methylbutan-2-yl)phenyl]prop-2-en-1-ol → 2-Methyl-3-[4-(2-methylbutan-2-yl)phenyl]propan-1-ol

https://huagongshe.com/reaction/1395218

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-3-[4-(2-methylbutan-2-yl)phenyl]prop-2-en-1-olHCID 57245577—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Product2-Methyl-3-[4-(2-methylbutan-2-yl)phenyl]propan-1-olHCID 20340528—

Reaction Steps

70 g of 3-(p-tert.amyl-phenyl)-2-methyl-allyl alcohol are dissolved in 700 ml of alcohol, treated with 7 g of 5% palladium/carbon and hydrogenated until the hydrogen uptake has been completed. The catalyst is subsequently filtered and the alcohol is evaporated. By distillation there is obtained pure 3-(p-tert.amyl-phenyl)-2-methyl-propanol of boiling point 124°-129° C./0.04 Torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04202894
Source datasetuspto-grants-1980_05
ORD IDord-a4457355c5234f16b2b7ac5c68dd416d
Source noteuspto-grants-1980_05