Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36552Generated: October 28, 2026

Butyl bromide → 4-Butoxy-3-methoxy-5-(prop-2-en-1-yl)benzaldehyde

https://huagongshe.com/reaction/36552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl bromideHCID 8002—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Allyl-4-hydroxy-5-methoxy-benzaldehydeHCID 1533806—
SolventWaterHCID 962—
Product4-Butoxy-3-methoxy-5-(prop-2-en-1-yl)benzaldehydeHCID 1993704798.8%

Reaction Steps

A mixture of 3-allyl-4-hydroxy-5-methoxybenzaldehyde (10.25 g, 0.053 mole), dimethylformanide (150 ml), potassium carbonate (8.29 g, 0.06 mole) and 1-bromobutane (8.22 g, 0.06 mole) was maintained at 40°-45° C. for three hours. The reaction mixture was plunged into iced water and the oil formed extracted with dichloromethane. After washing with water, drying and evaporation of the solvent, a brown oil was obtained which was passed through a bed of silica 60 to give a pale yellow oil, 3-allyl-4-butoxy-5-methoxybenzaldehyde (13 g, yield=91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05415854
Source datasetuspto-grants-1995_05
ORD IDord-ca49a5c4293049cba9d5b77a8d90c519
Source noteuspto-grants-1995_05