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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846685Generated: October 25, 2026

Hexamethylphosphoramide → Lithium cyclohexylisopropylamide

https://huagongshe.com/reaction/846685

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 numberUS05137915
Source datasetuspto-grants-1992_08
ORD IDord-295fd35276b54adf85d4bcdf365fd3b5
Source noteuspto-grants-1992_08