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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377626Generated: October 27, 2026

Water → 4-Methoxy-3-[6-(4-phenylbut-1-yloxy)hex-1-yloxy]benzaldehyde

https://huagongshe.com/reaction/377626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantIsovanillinHCID 12127—
Reactant1-[4-[(6-Bromohexyl)oxy]butyl]benzeneHCID 11012439—
SolventDimethylformamideHCID 6228—
Product4-Methoxy-3-[6-(4-phenylbut-1-yloxy)hex-1-yloxy]benzaldehydeHCID 1935626798.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 3-hydroxy-4-methoxybenzaldehyde (4.8 grams) in dimethylformamide (100 ml) at room temperature is added potassium carbonate (4.9 grams) and 1-bromo-6-(4-phenylbut-1-yloxy)hexane (10.0 grams). After stirring at 80° C. over 4 hours the reaction mixture is poured into water and extracted with ethyl acetate. The combined organics are washed with 1N sodium hydroxide and brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The resulting amber oil is filtered through a 5×10 cm pad of silica gel, eluting with a 1:3 mixture of ethyl acetate and hexane, to give 12.0 grams of a colorless oil. MS (m/z) 384.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028086
Source datasetuspto-grants-2000_02
ORD IDord-d9a5e50754914e5992451769dfb68347
Source noteuspto-grants-2000_02