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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452307Generated: October 30, 2026

Succinimide → HCID 19972706, compound

https://huagongshe.com/reaction/1452307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinimideHCID 11439—
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 3-methylflavone-8-carboxylateHCID 19972541—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 19972706HCID 1997270679.6%

Reaction Steps

A mixture of 9.2 g of ethyl 3-methyl-4-oxo-2-phenyl-4H-1-benzopyran-8-carboxylate (prepared as described by Da Re et al., J. Med. Chem., 2, 263 (1960)), 6.4 g of N-bromosuccinimide and 0.04 g of benzoylperoxide in 80 ml of anhydrous carbon tetrachloride was stirred at reflux for 1.5 hours. After cooling to room temperature the formed succinimide was collected by suction and washed with cold carbon tetrachloride. The mother liquors were evaporated to dryness in vacuo and the residue was rinsed with diethyl ether and collected by suction yielding 9.2 g of the title compound melting at 133°-134° C. after crystallization from acetone-n-hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05605896
Source datasetuspto-grants-1997_02
ORD IDord-53c993ec95574fd08462258c8e337c5b
Source noteuspto-grants-1997_02