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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874184Generated: October 31, 2026

N-bromobutanimide → HCID 67125220, compound

https://huagongshe.com/reaction/874184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 4-(2-chlorophenyl)-2-methylpyrimidine-5-carboxylateHCID 18981952—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 67125220HCID 67125220—

Reaction Steps

820 mg (2.96 mmol) of ethyl 4-(2-chlorophenyl)-2-methylpyrimidine-5-carboxylate and 633 mg (3.55 mmol) of N-bromosuccinimide were dissolved in 18 ml of carbon tetrachloride and, with stirring, heated to the boil. At boiling point, 49 mg (0.29 mmol) of 2,2′-azobis-2-methylpropionitrile were added a little at a time over a period of 5 hours, followed by refluxing for a further hour. After cooling to room temperature, the reaction solution was filtered and the mother liquor was freed from the solvent under reduced pressure. The desired product was isolated by chromatographic purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980886B2
Source datasetuspto-grants-2015_03
ORD IDord-f560c7d869f14d1fb147ae7209bc58bf
Source noteuspto-grants-2015_03