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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734707Generated: November 1, 2026

Hexamethylphosphoramide → Lithium cyclohexylisopropylamide

https://huagongshe.com/reaction/1734707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethylphosphoramideHCID 12679—
ReactantDiphenyl diselenideHCID 15460—
ReactantCyclohexylisopropylamineHCID 62386—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductLithium cyclohexylisopropylamideHCID 10877271—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534547
Source datasetuspto-grants-1996_07
ORD IDord-4368e7072326445a9b6f17ca861991f2
Source noteuspto-grants-1996_07