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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 846685생성일: 2026년 10월 25일

Hexamethylphosphoramide → Lithium cyclohexylisopropylamide

https://huagongshe.com/reaction/846685

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylphosphoramideHCID 12679—
반응물Diphenyl diselenideHCID 15460—
반응물CyclohexylisopropylamineHCID 62386—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물Lithium cyclohexylisopropylamideHCID 10877271—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05137915
출처 데이터셋uspto-grants-1992_08
ORD IDord-295fd35276b54adf85d4bcdf365fd3b5
출처 메모uspto-grants-1992_08