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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 846685Erstellt: 24. Oktober 2026

Hexamethylphosphoramide → Lithium cyclohexylisopropylamide

https://huagongshe.com/de/reaction/846685

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexamethylphosphoramideHCID 12679—
EduktDiphenyl diselenideHCID 15460—
EduktCyclohexylisopropylamineHCID 62386—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktLithium cyclohexylisopropylamideHCID 10877271—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05137915
Quelldatensatzuspto-grants-1992_08
ORD IDord-295fd35276b54adf85d4bcdf365fd3b5
Quellennotizuspto-grants-1992_08