Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110523Generated: November 2, 2026

Thionyl Chloride → 2-(3,4,5-trimethoxyphenyl)acetyl Chloride

https://huagongshe.com/reaction/2110523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3,4,5-Trimethoxyphenylacetic acidHCID 70372—
Product2-(3,4,5-trimethoxyphenyl)acetyl ChlorideHCID 11032124100%

Reaction Conditions

Temperature0 °C

Reaction Steps

3,4,5-trimethoxy phenyl acetic acid (9.5 g, 0.042 mol) was added slowly to the thionyl chloride (15 g, 0.126 mol) cooled to 0° C., and warmed to room temperature, then stirred for 3 hours. Residual thionyl chloride was distilled out to obtain 3,4,5-trimethoxy phenyl acetic acid chloride (10.3 g, 0.042 mol). Thymol (6.3 g, 0.042 mol) and triethylamine (6.4 g, 0.063 mol) were dissolved in 200 ml of dichloromethane and stirred, and then the above 3,4,5-trimethoxy phenyl acetic acid chloride (10.3 g) dissolved in 50 ml of dichloromethane was added thereto drop by drop. After the reaction was completed, reaction solution was condensed, and 500 ml of ethyl acetate was added to dissolve the reaction mixture. The resultant was washed with distilled water twice, dried with anhydrous sodium sulfate, then filtered and condensed, and finally proceeded to column chromatography to obtain 9.0 g (Yield=60%) of white solid state of the object product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517911B2
Source datasetuspto-grants-2009_04
ORD IDord-8b27ac2f69dd48589e4a1ca039702e2b
Source noteuspto-grants-2009_04