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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706376Generated: October 23, 2026

Sodium hydride → HCID 12807384, compound

https://huagongshe.com/en/reaction/1706376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantLomifyllineHCID 65599—
ReactantMethylenetriphenylphosphoraneHCID 137960—
ReactantMethyltriphenylphosphonium iodideHCID 638159—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 12807384HCID 12807384—

Reaction Conditions

Temperature80 °C

Reaction Steps

0.5 g of sodium hydride are reacted with 15 ml of anhydrous dimethyl-sulphoxide under a nitrogen atmosphere with stirring at 80° C. and cooled to 15° C. after 25 minutes. To prepare triphenyl-methylene-phosphorane, 8.1 g of methyl-triphenyl phosphonium iodide in 20 ml of anhydrous dimethyl-sulphoxide are added to this solution. After stirring for 10 minutes at room temperature, 5.6 g of 1,3-dimethyl-7-(5-oxohexyl)-xanthine in 10 ml of dimethylsulphoxide are added dropwise over 10 minutes, and the temperature is not allowed to exceed 20° C. After standing overnight, the mixture is dissolved in water, extracted with diethyl ether and the ether phase is separated and dried over Na2SO4. The product obtained after evaporation at reduced pressure is subsequently subjected to a purification by column chromatography on silica gel with methylene chloride/acetone (1:1) as eluent. The resulting product is in the form of an oil after distillation under reduced pressure. Yield: 3.5 g (63.3% of theory relative to the starting product used); refractive index: nD20 =1.5445.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207321
Source datasetuspto-grants-1980_06
ORD IDord-e12a492265e849b391491de412a086cb
Source noteuspto-grants-1980_06