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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706373Generated: November 2, 2026

Sodium Hydroxide → HCID 20157766, compound

https://huagongshe.com/reaction/1706373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHomoallyl bromideHCID 21241—
Reactant1,3-DibutylxanthineHCID 101421—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
ProductHCID 20157766HCID 20157766—

Reaction Conditions

Temperature70 °C

Reaction Steps

38.9 g of 1,3-di-n-butyl-xanthine are added at 25° C. to a solution of 3.4 g of sodium in 200 ml of absolute ethanol. 20.5 g of 4-bromobut-1-ene are then added at 50° C. After stirring for 46 hours under a nitrogen atmosphere at 70° C. the reaction mixture is cooled to 20° C., precipitated sodium bromide is filtered off and the filtrate is then evaporated under reduced pressure. The residue obtained is treated with chloroform and 1 N sodium hydroxide solution to remove 1,3-di-n-butyl-xanthine. From the chloroform phase there is obtained a yellow oily residue which after column chromatography on silica gel with methylene chloride/acetone (8:2) as eluent and after distillation under reduced pressure yields 29.7 g (78.8% of theory relative to reacted 1,3-di-n-butyl-xanthine) of the title compound with a melting point of 41° to 42° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207321
Source datasetuspto-grants-1980_06
ORD IDord-a09f82ff04d146ce86564c0fbf6d72c5
Source noteuspto-grants-1980_06