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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733273Generated: October 26, 2026

2-Propenal, 3-[4-(1,1-dimethylethyl)phenyl]-2-methyl- → 3-(4-tert-Butylphenyl)-2-methylprop-2-en-1-ol

https://huagongshe.com/reaction/1733273

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Propenal, 3-[4-(1,1-dimethylethyl)phenyl]-2-methyl-HCID 114659—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product3-(4-tert-Butylphenyl)-2-methylprop-2-en-1-olHCID 54381367—

Reaction Steps

404.5 g of 3-(p-tert.butyl-phenyl)-2-methyl-acrolein are dissolved in 2500 ml of methanol and treated portionwise with 38 g of sodium borohydride while cooling with ice. Subsequently, the mixture is stirred at room temperature for 2.5 hours, poured into 2500 ml of ice-cold 2-N hydrochloric acid and exhaustively extracted with hexane. The combined hexane extracts are washed neutral with water, dried over sodium sulphate and evaporated. Vacuum distillation yields pure 3-(p-tert.butyl-phenyl)-2-methyl-allyl alcohol of boiling point 119° C./0.005 Torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04241058
Source datasetuspto-grants-1980_12
ORD IDord-c9b3e26ab02241aaa76378731f7f9858
Source noteuspto-grants-1980_12