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HRID 4979作成日:2026年10月23日

2-(2-Chlorobenzylidene)-1-azabicyclo[2.2.2]octan-3-one → 2-[(2-Chlorophenyl)phenylmethyl]-1-azabicyclo[2.2.2]octan-3-one

https://huagongshe.com/ja/reaction/4979

反応式

関与物質

役割名称HCID仕込み量
反応物2-(2-Chlorobenzylidene)-1-azabicyclo[2.2.2]octan-3-oneHCID 297405—
反応物HCID 178418255HCID 178418255—
溶媒TolueneHCID 1140—
生成物2-[(2-Chlorophenyl)phenylmethyl]-1-azabicyclo[2.2.2]octan-3-oneHCID 19797478—

反応手順

2-(2-Chlorobenzylidene)-1-azabicyclo[2.2.2]octan-3-one (3 g) was dissolved in toluene (30 ml) and placed in a dropping funnel. Phenylmagnesium bromide was dissolved in toluene (15 ml) and stirred under nitrogen. This was cooled in an ice/water bath and the benzylidene solution was added dropwise. After 3 hrs the reaction was quenched with ammonium chloride solution and the aqueous layer extracted with dichloromethane (×4); this was combined with the original toluene layer and dried (MgSO4). The solvent was removed in vacuo and the residue purified by chromatography on silica eluting with 1:1 hexane:diethyl ether which afforded the title compound as a 2:1 mixture of its diastereoisomers:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05242930
出典データセットuspto-grants-1993_09
ORD IDord-28e88db65242445cb373f341e46ba373
出典メモuspto-grants-1993_09