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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531736Generated: October 31, 2026

Ethyl bromoacetate → HCID 53936007, compound

https://huagongshe.com/reaction/1531736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantHCID 21250244HCID 21250244—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53936007HCID 53936007—

Reaction Steps

2.0 g (4.15 mmol) of 4-{[6-(quinolin-8-yl-sulphonylamino)-1-methyl-2-oxo-1,2-dihydroquinoxalin-3-yl]-methyl}-benzonitrile are dissolved in 150 ml tetrahydrofuran and after the addition of 0.2 g (4.15 mmol) of sodium hydride (50% in oil) stirred for 2 hours at ambient temperature. After the addition of 0.47 ml (4.15 mmol) of ethyl bromoacetate the reaction mixture was stirred for 5 hours. The precipitate is suction filtered, the mother liquor is evaporated down and chromatographed on silica gel, eluting initially with petroleum ether and then with petroleum ether/ethyl acetate (55:45). The desired fractions are combined and evaporated down.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200976B1
Source datasetuspto-grants-2001_03
ORD IDord-588be961b5754a3ea71ba4e0da021a49
Source noteuspto-grants-2001_03