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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293675Generated: October 31, 2026

4-Ethylbenzaldehyde → 4-Ethyl-α-propylbenzenemethanol

https://huagongshe.com/reaction/2293675

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-EthylbenzaldehydeHCID 20861—
ReactantHCID 178455851HCID 178455851—
SolventDiethyl EtherHCID 3283—
Product4-Ethyl-α-propylbenzenemethanolHCID 22486907—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a flame-dried flask under an argon atmosphere is added 0.69 mL of commercially available 4-ethylbenzaldehyde and charged with 15 mL of diethyl ether. The solution is cooled to 0° C. and is treated with 3.0 mL (2.0M in diethyl ether) of propylmagnesium bromide. The reaction mixture is left to warm to room temperature overnight and then quenched by the addition of aqueous ammonium chloride. After dilution with diethyl ether the phases are separated; the organic layer is washed with saturated ammonium chloride, dried (magnesium sulfate) and finally concentrated under reduced pressure. The residue is flash column chromatographed using 25% to 30% diethyl ether in hexane to yield 1.08 g of the title product as a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686486
Source datasetuspto-grants-1997_11
ORD IDord-010768999b264906882c5e797d45e26d
Source noteuspto-grants-1997_11