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HRID 40641作成日:2026年10月23日
Diisobutylaluminum hydride → Z-(1S,6S)-7-(2,4-Dimethoxy-benzyl)-9-naphthalen-2-yl-7,9-diaza-bicyclo[4.2.2]dec-3-ene
https://huagongshe.com/ja/reaction/40641
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Diisobutylaluminum hydride | HCID 14487 | — |
| 反応物 | Z-(1S,6S)-7-(2,4-Dimethoxy-benzyl)-9-naphthalen-2-yl-7,9-diaza-bicyclo[4.2.2]dec-3-ene-8,10-dione | HCID 69230528 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Z-(1S,6S)-7-(2,4-Dimethoxy-benzyl)-9-naphthalen-2-yl-7,9-diaza-bicyclo[4.2.2]dec-3-ene | HCID 59686812 | — |
反応手順
Z-(1S,6S)-7-(2,4-Dimethoxy-benzyl)-9-naphthalen-2-yl-7,9-diaza-bicyclo[4.2.2]dec-3-ene-8,10-dione (102 mg, 0.023 mmol), THF (1 mL) and DiBAl-H (6 mL, 6 mmol, [1M]) were placed in a μW tube under argon vent then heated to 130° C. for 900 sec. The reaction was quenched with Rochelle's solution and diethyl ether and the resulting mixture stirred overnight. The organic layer was separated and dried with magnesium sulfate, filtered and the solvent evaporated under reduced pressure to yield a crude oil, which was purified via reverse chromatography (20% CH3CN/water to 100% water) to yield the title compound as a residue.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08530475B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-9a469fa7f5324139bbfd8a68ecc1fe1c |
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| 出典メモ | uspto-grants-2013_09 |
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