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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664214Generated: November 1, 2026

Thionyl Chloride → 3-Allyloxy-5-chlorocarbonyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1664214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant5-Allyloxy-isophthalic acid monomethyl esterHCID 21942537—
Product3-Allyloxy-5-chlorocarbonyl-benzoic acid methyl esterHCID 21942493—

Reaction Steps

A solution of 2.17 g (9.18 mmol) of 5-allyloxy-isophthalic acid monomethyl ester in 9.2 ml of thionyl chloride is heated to reflux for 1 h. Excess thionyl chloride is removed under reduced pressure to yield 3-allyloxy-5-chlorocarbonyl-benzoic acid methyl ester in the form of a color-less oil, which is used without further purification. To a solution of 2.36 g (9.18 mmol) of 3-allyloxy-5-chlorocarbonyl-benzoic acid methyl ester in 9 ml of DCM 27.6 ml of a 1 M solution of dimethylamine in THF (3 eq.) are added at 0° C. The mixture is stirred at rt for 2 h. 100 ml of a half-saturated aq ammonium chloride solution are added. The mixture is extracted with TBME (2×75 ml), and the combined organic layers are washed with 50 ml of water, dried over sodium sulfate and evaporated. The residue is purified by chromatography on silica gel (EtOAc) to give the product as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039455B2
Source datasetuspto-grants-2011_10
ORD IDord-297d210e54554450b7298216bab1f86d
Source noteuspto-grants-2011_10