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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612521Generated: October 30, 2026

Water → HCID 67587072, compound

https://huagongshe.com/reaction/612521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantAzlactoneHCID 65073—
ReactantHCID 11748443HCID 11748443—
CatalystTitanium TetrachlorideHCID 24193—
SolventCarbon TetrachlorideHCID 5943—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67587072HCID 6758707222.9%

Reaction Steps

A solution of 11 ml of titanium tetrachloride in 27 ml of carbon tetrachloride is added dropwise at -10° C. to 110 ml of anhydrous tetrahydrofuran. Once the addition is complete, a solution of 14.7 g of 4-chloro-4'-(methylsulphonyl)benzophenone (the preparation of which is described in the document W097/37984) in 50 ml of anhydrous tetrahydrofuran is added dropwise in keeping the temperature below 0° C. A mixture of 8.05 g of 2-phenyl-5(4H)-oxazolone, 16 ml of pyridine and 25 ml of anhydrous tetrahydrofuran is then added dropwise at 0° C. The mixture is stirred 2 hours at this temperature, then brought to ambient temperature and 50 ml of water are added. After decanting, the organic phase is washed with water then dried over magnesium sulphate and evaporated off under vacuum. The residue crystallises in an acetone/t-butyl methyl ether mixture and is chromatographed on silica in an acetone/dichloromethane mixture (0.3/10) to give 5 g of (E)-4-[1-(4-chlorophenyl)-1-[4-(methylsulphonyl)phenyl]methylene]-2-phenyl-5-oxazolone as crystals of melting point 226° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06004994
Source datasetuspto-grants-1999_12
ORD IDord-98c5581e60104249889dded1edca963f
Source noteuspto-grants-1999_12