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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248112Generated: October 31, 2026

Ethyl bromoacetate → HCID 54416269, compound

https://huagongshe.com/reaction/1248112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodiumHCID 5360545—
ReactantHCID 19848359HCID 19848359—
SolventMethanolHCID 887—
ProductHCID 54416269HCID 5441626964.5%

Reaction Steps

22.5 g (0.1 mol) of 3-hydroxy-2,4,6-trichlorobenzonitrile are dissolved in 240 ml of methanol with the addition of 2.3 g (0.1 mol) of metallic sodium. To the resultant suspension of the sodium salt is added 12.15 ml (0.11 mol) of ethyl bromoacetate, and the reaction mixture is heated to reflux until solution is complete. After filtration over active carbon, the solution is cooled and stirred for several hours in an ice bath. The resultant crystalline precipitate is vacuum-filtered, washed with a little ice-cold methanol and dried at 50° C., to produce 19 g (64.5% of theory) of 3-cyano-2,4,6-trichlorophenoxyacetic acid methyl ester as a white powder, mp 110°-112° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04522839
Source datasetuspto-grants-1985_06
ORD IDord-6c8d60f74f604d0fa439100039b3ecf1
Source noteuspto-grants-1985_06