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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23588Generated: October 25, 2026

Allyl Alcohol → (3,4-Dichloro-phenoxy)-acetic acid allyl ester

https://huagongshe.com/reaction/23588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
Reactant(3,4-Dichlorophenoxy)acetic acidHCID 11495—
Product(3,4-Dichloro-phenoxy)-acetic acid allyl esterHCID 6973216096.8%

Reaction Steps

To a solution of commercially available (3,4-dichloro-phenoxy)-acetic acid (2.65 g, 12.0 mmol) in allyl alcohol (12.0 cm3, 180 mmol) at ambient temperature under an atmosphere of dry nitrogen was added 4 drops concentrated sulfuric as a catalyst. The solution was stirred at ambient temperature for 20 hours and the volatile fractions removed in vacuo. The residue was dissolved in ethyl ether (50 cm3), washed with water (25 cm3), washed with saturated sodium bicarbonate (25 cm3), washed with brine (25 cm3), dried over magnesium sulfate, vacuum filtered and the filtrate volatile fractions removed in vacuo to afford the title compound as a colorless viscous oil (3.02 g, 96.8%) with positive ion ESI (M+H)+261.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852713B2
Source datasetuspto-grants-2005_02
ORD IDord-603affca2e4842b7b2bec7915cb213f2
Source noteuspto-grants-2005_02