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HRID 485373作成日:2026年10月25日

Sodium hydride → 2,3-dihydro-1-methylene-1H-pyrrolizine

https://huagongshe.com/reaction/485373

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物3H-1,2-dihydro-1-pyrrolizinoneHCID 97347—
反応物MethylenetriphenylphosphoraneHCID 137960—
触媒Methyltriphenyliphosphonium bromideHCID 74505—
溶媒Dimethyl SulfoxideHCID 679—
生成物2,3-dihydro-1-methylene-1H-pyrrolizineHCID 20270355—

反応手順

A solution of 2,3-dihydro-1-oxo-1H-pyrrolizine (16.1 g, 0.133 m); J. Org. Chem., 27 2468 (1962) ) in dried dimethylsulfoxide (60 ml) is added dropwise over ca. 10 minutes to a mixture of methylenetriphenylphosphorane (from methyl triphenylphosphonium bromide (57.2 g, 0.16 m), sodium hydride 60% dispersion (6.4 g, 0.16 m) and dimethylsulfoxide (256 ml) in the standard fashion (J. Org. Chem., 28 1128 (1963)) at ambient temperatures. After stirring for ca 2 hours, the mixture is heated in an oil-bath set at 70° C. for ca 30 minutes, and let cool. After stirring overnight at ambient temperatures, the mixture is poured into 1200 ml of ice-water, extracted 4×400 ml of ether, the ether layers washed 3×400 ml of water, dried and concentrated to a residue. The residue is extracted well with hexane, the filtered hexane extracts concentrated and distilled to yield 2,3-dihydro-1-methylene-1H-pyrrolizine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04536512
出典データセットuspto-grants-1985_08
ORD IDord-4158bf6627e24c25875e6801c3c29dee
出典メモuspto-grants-1985_08