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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568644Generated: October 30, 2026

Ethyl bromoacetate → HCID 13015695, compound

https://huagongshe.com/reaction/568644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
ReactantHCID 135589642HCID 135589642—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 13015695HCID 13015695—

Reaction Conditions

Temperature65 °C

Reaction Steps

7-chloro-6-hydroxy-3-(2-pyridyl)-1,2-benzisoxazole (10.0 g) is dissolved in 80 ml of DMF and added to an ice cold suspension of NaH (1.1 g) in 50 ml of DMF. When hydrogen evolution ceases, ethyl bromoacetate (7.5 g) in 20 ml of DMF is added. After an additional 90 minutes, 200 ml of H2O and 10 ml of 50% NaOH are added and the reaction warmed at 65° C. for 45 minutes. The mixture is poured into H2O, acidified to pH 1-2, and a solid product filtered and dried to give {[7-chloro-3-(2-pyridyl)-1,2-benzisoxazole-6-yl]oxy}acetic acid, mp 255°-256° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04728662
Source datasetuspto-grants-1988_03
ORD IDord-102ad08aa569468780a3f3656fd12b54
Source noteuspto-grants-1988_03