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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109042Generated: October 25, 2026

Chloroacetic Acid → 2-(2-(Benzyloxy)ethoxy)acetic acid

https://huagongshe.com/reaction/2109042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
Reactant2-(Benzyloxy) ethanolHCID 12141—
ReactantSodium hydrideHCID 24758—
SolventDimethylacetamideHCID 31374—
Product2-(2-(Benzyloxy)ethoxy)acetic acidHCID 21790136102.4%

Reaction Steps

Sixty % sodium hydride in oil (6.80 g) is suspended in N,N-dimethylacetamide (80 ml) and a solution of 2-(benzyloxy)ethanol (12.9 g) in N,N-dimethylacetamide (50 ml) is added dropwise to the mixture over 10 minutes under ice-cooling. After stirring at room temperature for 15 minutes, the reaction solution is cooled with ice, and thereto is added chloroacetic acid (8.13 g) in small portions. The mixture is then stirred at room temperature for 11 hours. The reaction solution is concentrated under reduced pressure, and to the resulting residue is added aqueous sodium hydrogen carbonate solution and the mixture is washed with diethyl ether. The aqueous layer is acidified with conc. hydrochloric acid, and then extracted with ethyl acetate. The organic layer is washed with saturated brine, dried over sodium sulfate and evaporated to remove solvent under reduced pressure to give [2-(benzyloxy)ethoxy]acetic acid (18.24 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514449B2
Source datasetuspto-grants-2009_04
ORD IDord-5521e11f5a2a47bc848cb3edd31cc217
Source noteuspto-grants-2009_04