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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899151Generated: October 29, 2026

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

https://huagongshe.com/reaction/1899151

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 numberUS05571814
Source datasetuspto-grants-1996_11
ORD IDord-94b3d336e6d44842aac297902c3913ff
Source noteuspto-grants-1996_11