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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739248Generated: November 1, 2026

Acetovanillone → (Z)-1-[4-[(4-chloro-2-butenyl)oxy]-3-methoxyphenyl]ethanone

https://huagongshe.com/reaction/1739248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetovanilloneHCID 2214—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-Dichloro-cis-2-buteneHCID 6432115—
SolventAcetonitrileHCID 6342—
Product(Z)-1-[4-[(4-chloro-2-butenyl)oxy]-3-methoxyphenyl]ethanoneHCID 57454977106.8%

Reaction Steps

A stirred mixture of 4-hydroxy-3-methoxyacetophenone (16.6 g, 10 mmole), K2CO3 (14 g, 100 mmol) and cis-1,4-dichloro-2-butene (Aldrich, 15 g, 120 mmol) in acetonitrile (250 ml) was heated at reflux for 2.5 hours. The mixture was filtered and concentrated to an oil. Purification was by flash chromatography. The fractions containing the purest product were combined and concentrated to give white crystals, 7.7 g, 30%. This was recrystallized from ether to give analytical pure (Z)-1-[4-[(4-chloro-2-butenyl)oxy]-3-methoxyphenyl]ethanone (2.72 g), m.p.=64-66° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965546
Source datasetuspto-grants-1999_10
ORD IDord-1a05e2089cb0442e9fa035ff731c4ca2
Source noteuspto-grants-1999_10