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HRID 1602129作成日:2026年10月25日

Diethyl Ether → A 802715

https://huagongshe.com/reaction/1602129

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物PropentofyllineHCID 4938—
反応物Ammonium ChlorideHCID 25517—
反応物HCID 178418332HCID 178418332—
溶媒TetrahydrofuranHCID 8028—
生成物A 802715HCID 129959—

反応手順

22.4 g (0.3 mol) of methylmagnesium chloride in the form of a 20% strength solution in tetrahydrofuran are added dropwise with vigorous stirring at room temperature to a suspension of 61.3 g (0.2 mol) of 3-methyl-1-(5-oxohexyl)-7-propylxanthine in 2 1 of anhydrous ether, the internal temperature rising to approximately 30° C. The mixture is then warmed with stirring and under reflux for 2 hours, treated with saturated aqueous ammonium chloride solution to decompose the alkoxide formed, and the organic phase is separated off and washed twice with 500 ml of water each time. The collected water phases are extracted thoroughly with dichloromethane again. The dichloromethane extract is combined with the ethereal phase, dried over sodium sulfate, filtered and evaporated under reduced pressure, 59.0 g of crude product (91.5% of theory) being obtained, which is purified by recrystallization from diisopropyl ether.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05981536
出典データセットuspto-grants-1999_11
ORD IDord-6ed7cf8995a548398f2f224903274b33
出典メモuspto-grants-1999_11