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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109603Generated: November 2, 2026

Diethyl bromomalonate → HCID 20144889, compound

https://huagongshe.com/reaction/1109603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl bromomalonateHCID 69637—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 11446993HCID 11446993—
SolventDichloromethaneHCID 6344—
ProductHCID 20144889HCID 20144889—

Reaction Steps

ca) 8.05 g of 3,4-dihydro-thieno[2,3-f][1,4]thiazepine-5(2H)-thione were suspended in 40 ml of methylene chloride and treated under argon with a solution of 7.1 ml of diethyl bromomalonate in 40 ml of methylene chloride. After stirring for 2.5 hours, 50 ml of 10 percent potassium hydrogen carbonate solution were added thereto and the mixture was stirred for 30 minutes. The organic phase was separated and the aqueous phase was extracted twice with methylene chloride. After drying with sodium sulfate, the extract was chromatographed on silica gel, whereby diethyl [3,4-dihydrothieno[2,3-f][1,4]thiazepine-8-(5H)-ylidene]malonate was obtained in the form of slightly yellowish crystals of m.p. 87°-89° (cyclohexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05321021
Source datasetuspto-grants-1994_06
ORD IDord-4bee68bc5f124631bf879b6510d3ad17
Source noteuspto-grants-1994_06