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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484317Generated: October 31, 2026

Ethyl bromoacetate → HCID 54519729, compound

https://huagongshe.com/reaction/484317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantTriethylamineHCID 8471—
ReactantHCID 19747228HCID 19747228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54519729HCID 5451972997.2%

Reaction Steps

Dry THF (20 ml) was added to 0.4 g of 8-cyano-11-(4-piperidylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine to dissolve the latter, followed by the addition of 0.2 g of triethylamine and 0.27 g of ethyl bromoacetate. The resultant mixture was stirred at room temperature for 24 hours. After the completion of the reaction, THF was distilled off under reduced pressure, the residue was dissolved in chloroform, and the resultant solution was washed with water. The chloroform layer was dried over anhydrous Na2SO4 and then filtered. The chloroform was distilled off under reduced pressure. The residue was purified by chromatography on a silica gel column and, from relevant fractions eluted with chloroform:methanol (20:1), 0.5 g of 8-cyano-11-(1-ethoxycarbonylmethyl-4-piperidylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine was obtained (yield: 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05231101
Source datasetuspto-grants-1993_07
ORD IDord-5459fe61ea8540e8b176ecb30a487379
Source noteuspto-grants-1993_07