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HRID 83986作成日:2026年10月26日

Sodium bis(2-methoxyethoxy)aluminiumhydride → 5-Chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]

https://huagongshe.com/reaction/83986

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
反応物1-Methanesulfonyl-5-chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]HCID 68924239—
溶媒TolueneHCID 1140—
生成物5-Chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]HCID 6893064974.7%

反応条件

温度100 °C

反応手順

A solution of 1-methanesulfonyl-5-chloro-1′-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3′-pyrrolidine] obtained in Step D (256 mg) in toluene (25 ml) under argon was treated with sodium bis(2-methoxyethoxy)aluminium hydride (Red-Al, 65% in toluene, 0.67 ml) and the reaction mixture was stirred at 100° C. for 1 hour, cooled to room temperature, quenched by addition of ethyl acetate (10 ml), stirred for 15 min and concentrated in vacuo. The residue was purified by silica gel chromatography (eluent ethyl acetate:methanol 95:5) to afford 5-chloro-1′-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3′-pyrrolidine] (157 mg) as a yellow oil, which was characterised by its mass and NMR spectra.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846907B2
出典データセットuspto-grants-2014_09
ORD IDord-8798f0c9457348929512f941c499cc49
出典メモuspto-grants-2014_09