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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373535Generated: October 30, 2026

Propionyl chloride → HCID 131717641, compound

https://huagongshe.com/reaction/373535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionyl chlorideHCID 62324—
ReactantHCID 131717642HCID 131717642—
SolventPyridineHCID 1049—
ProductHCID 131717641HCID 131717641—

Reaction Conditions

Temperature0 °C

Reaction Steps

A quantity of 1.29 g of 1-phenyl-3-methylallyl-barbituric acid prepared as described in Example Ia) is dissolved in 10 ml of pyridine. 0.52 ml of propionyl chloride is added dropwise to this solution which is cooled at 0° C. The reaction mixture is stirred at approximately 0° C. for 30 minutes and then at room temperature for 3 hours, and is then poured on 50 ml of ice water. After stirring with active carbon and filtering, the filtrate is acidified with conc. hydrochloric acid and extracted with methylene chloride. The organic layer is separated, washed with water, dried and evaporated. The final product is purified by means of column chromatography: silica gel/methylene chloride. The title compound is obtained in a yield of 0.65 g; melting-point 76°-80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05164396
Source datasetuspto-grants-1992_11
ORD IDord-17bf1731d3ea426cb2d90a3733bf67e6
Source noteuspto-grants-1992_11