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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296496Generated: October 30, 2026

Ethyl bromoacetate → HCID 19848366, compound

https://huagongshe.com/reaction/2296496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodiumHCID 5360545—
ReactantHCID 19848356HCID 19848356—
SolventMethanolHCID 887—
ProductHCID 19848366HCID 1984836684.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

16 g (66.9 mmol) of 3-hydroxy-2,4,6-trichlorobenzamide is suspended in 100 ml of methanol and dissolved by adding 1.54 g (66.9 mmol) of sodium. After the addition of 16.8 g (66.9 mmol) of bromoacetic acid ethyl ester, the mixture is maintained under reflux until the reaction is complete (TLC control). The product is then concentrated to dryness under vacuum and the resultant 3-carbamoyl-2,4,6-trichlorophenoxyacetic acid methyl ester is suspended in 100 ml of water. The mixture is combined with 20 ml of concentrated sodium hydroxide solution and maintained for 3 hours at 60° C. for saponifying. The solution is filtered over active carbon, brought to pH 2 by adding concentrated hydrochloric acid, and the precipitate is vacuum-filtered after several hours of stirring in an ice bath. After washing with water and drying, 16.8 g (84% of theory) of 3-carbamoyl-2,4,6-trichlorophenoxyacetic acid is obtained as a white powder, mp 261°-262° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04429152
Source datasetuspto-grants-1984_01
ORD IDord-0f6f7de4a12c4c118651fa634e2f78d3
Source noteuspto-grants-1984_01