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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483803Generated: October 25, 2026

Water → HCID 19043035, compound

https://huagongshe.com/reaction/483803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4,4'-DibromobenzophenoneHCID 72868—
Reactant5-BromopyrimidineHCID 78344—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 19043035HCID 19043035—

Reaction Steps

A solution of 20 ml of 1.6N n-butyllithium in hexane is added dropwise within 30 minutes, with stirring and with the exclusion of moisture, to a solution, cooled to -75°, of 5.2 g (33 mmol) of 5-bromopyrimidine and 10.7 g (31.2 mmol) of 4,4'-dibromobenzophenone in 130 ml of THF. The reaction mixture is stirred for a further 0.5 hour at -75° and then for 16 hours at room temperature; then, while cooling with ice, it is hydrolysed by adding 20 ml of water. The organic phase is separated and diluted with ethyl acetate. The solution is washed with 2N HCl and a semi-saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated by evaporation. The residue is purified by column chromatography (400 g of silica gel, methylene chloride/ethyl acetate 85:15) and recrystallised from ethyl acetate, m.p. 89°-90°, Rf value=0.11 (silica gel, methylene chloride/ethyl acetate 85:15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05227393
Source datasetuspto-grants-1993_07
ORD IDord-d1218f6eacb444768780ec2eb689daa7
Source noteuspto-grants-1993_07