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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199705Generated: October 30, 2026

Ethyl bromoacetate → 2-(trans-3-Ethoxycarbonylmethoxystyryl)benzothiazole

https://huagongshe.com/reaction/1199705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 7986269HCID 7986269—
SolventAcetoneHCID 180—
Product2-(trans-3-Ethoxycarbonylmethoxystyryl)benzothiazoleHCID 1405117577%

Reaction Steps

To 30 ml of acetone were added 200 mg of 2-(trans-3-hydroxystyryl)benzothiazole, 0.11 ml of ethyl bromoacetate and 131 mg of potassium carbonate, and the mixture was refluxed for 4 hours. After cooled to room temperature, the mixture was extracted with ethyl ether, dried over anhydrous magnesium sulfate and then the solvent was evaporated under reduced pressure. After the crude crystals of the residue were washed with ethyl ether and n-hexane, they were dried under reduced pressure to give 207 ml (yield 77%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04902700
Source datasetuspto-grants-1990_02
ORD IDord-33abe700bcb745738dd16b41f5f9c8a4
Source noteuspto-grants-1990_02