戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 846685作成日:2026年10月27日

Hexamethylphosphoramide → Lithium cyclohexylisopropylamide

https://huagongshe.com/reaction/846685

反応式

関与物質

役割名称HCID仕込み量
反応物HexamethylphosphoramideHCID 12679—
反応物Diphenyl diselenideHCID 15460—
反応物CyclohexylisopropylamineHCID 62386—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Lithium cyclohexylisopropylamideHCID 10877271—

反応手順

Lithium cyclohexylisopropylamide was prepared from cyclohexylisopropylamine (0.07 ml) and n-butyllithium (1.6-M, 0.265 ml) in THF (1 ml). To the resultant was added dropwise a solution of methyl ester (34) (0.1412 g) in THF (4 ml) and stirred for 2 hours. A solution of diphenyl diselenide (0.132 g) and HMPA (0.074 ml) in THF (2 ml) was added, and the mixture was stirred at -70° C. for one hour and -40° C.--30° C. for 1.5 hours. According to the conventional treatment, selenide (35) (0.1247 g) was obtained. Selenide (35) (0.1247 g) was dissolved in ethyl acetate (6 ml) and methanol (4 ml), and stirred at room temperature with aqueous hydrogen peroxide (30%) (0.5 ml) for one hour. The crude product obtained by the conventional treatment was chromatographed (ethyl acetate/hexane (1:6)) to give Δ2 -PGE2 α-methyl ester (36). Yield, 0.091 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05137915
出典データセットuspto-grants-1992_08
ORD IDord-295fd35276b54adf85d4bcdf365fd3b5
出典メモuspto-grants-1992_08