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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771145Generated: November 2, 2026

Vanillin → 4-isobutoxy-3-methoxybenzaldehyde

https://huagongshe.com/reaction/1771145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVanillinHCID 1183—
Reactant1-Bromo-2-methylpropaneHCID 6555—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product4-isobutoxy-3-methoxybenzaldehydeHCID 673697—

Reaction Steps

In 250 ml three necked flask, equipped with reflux condenser, mechanical stirrer, 30.4 g (200 mmol) of vanillin, 28 g (200 mmol) of dry K2CO3 and 150 ml of abs. dimethylformamide are placed in the flow of argon. The mixture is stirred for 20 min in argon condition, then 34.3 g (250 mmol) of isobutyl bromide is added. The mixture is refluxed with stirring in argon condition for 20 h at 90÷100° C., and concentrated in vacuum at 50÷80° C. to dryness. Then 200 ml of water is added to the residue, the mixture is extracted with (4×100 ml) of dichloromethane. The combined organic fraction is washed with 7% NaOH solution, dried over magnesium sulfate, filtered off, concentrated in vacuum at 50÷80° C. The residue (15 g of brown oil)-crude 4-(2-methylpropyloxy)-3-methoxybenzaldehyde is used on the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249115B2
Source datasetuspto-grants-2016_02
ORD IDord-bdb7e2433d5e4621ab36f3716ba27e03
Source noteuspto-grants-2016_02