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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium bis(2-methoxyethoxy)aluminiumhydride | HCID 21584525 | — |
| 反応物 | 1-Methanesulfonyl-5-chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine] | HCID 68924239 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 5-Chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine] | HCID 68930649 | 74.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846907B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-8798f0c9457348929512f941c499cc49 |
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| 出典メモ | uspto-grants-2014_09 |
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