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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594640Generated: October 30, 2026

Chloroacetic Acid → (2,6-Dimethylphenoxy)acetic acid

https://huagongshe.com/reaction/1594640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
ReactantPhenolHCID 996—
Reactant2,6-DimethylphenolHCID 11335—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
Product(2,6-Dimethylphenoxy)acetic acidHCID 101369—

Reaction Steps

2,6-Dimethylphenol (102.8 g, 0.842 mol) and chloroacetic acid (159.6 g, 1.68 mol) in 1000 ml of H2O was added to a 3-L, 3-necked round bottom flask with mechanical stirring and a water-cooled condenser. A solution of NaOH (134.9 g, 3.37 mol) dissolved in 500 ml of water was slowly added to the above mixture via addition funnel and heat to reflux. After 2 hours, additional chloroacetic acid (79.4 g, 0.84 mol) and NaOH solution (67.2 g, 1.68 mol in in 200 ml water) was added to the reaction mixture. After 19 hours, additional chloroacetic acid (39.8 g, 0.42 mol) and NaOH solution (33.6 g, .84 mol in in 100 ml water) was added to the reaction mixture and refluxing was continued until starting phenol was consumed. The reaction flask was cooled in and ice-water bath and acidified to pH=1 with conc. HCl, causing a precipitate to form. The resulting slurry was stirred in the ice bath for 1 hour then filtered. The solid was dissolved in hot (100° C.) water and cooled to crystallize the product as white plates, mp=136-137° C., yield =78.8 9, 52%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284767B1
Source datasetuspto-grants-2001_09
ORD IDord-6cdb6e5fbb0346e498614045beb0e3e0
Source noteuspto-grants-2001_09