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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259887Generated: November 4, 2026

Succinimide → HCID 19972706, compound

https://huagongshe.com/reaction/2259887

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 numberUS05474994
Source datasetuspto-grants-1995_12
ORD IDord-651d1ae8d0484ea994df88b94093c0f0
Source noteuspto-grants-1995_12