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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953295Generated: November 3, 2026

Ethyl bromoacetate → HCID 86755732, compound

https://huagongshe.com/reaction/1953295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 23302733HCID 23302733—
SolventEthyl AcetateHCID 8857—
ProductHCID 86755732HCID 86755732—

Reaction Steps

1.0 g (2 mmol) of 4-[(6-(quinolin-8-yl-sulphonylamino)-3-bromo-benzofuran-2-yl)-methyl]-benzonitrile are dissolved in 20 ml absolute tetrahydrofuran and after the addition of 100 g (2 mmol) of sodium hydride (50% in oil) stirred for 20 minutes at ambient temperature. Then 0.22 ml (2 mmol) of ethyl bromoacetate are added under a nitrogen atmosphere. The reaction mixture is refluxed for 6 hours, cooled, diluted with ethyl acetate and washed with sodium chloride solution. The combined organic extracts are dried and concentrated by evaporation. The residue is chromatographed on silica gel and eluted with petroleum ether/ethyl acetate (90:10 and 75:25). The desired fractions are combined and concentrated by evaporation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114532
Source datasetuspto-grants-2000_09
ORD IDord-125db66e8918491894a8cf739cd878e8
Source noteuspto-grants-2000_09