関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 反応物 | (E)-N-(4'-chlorobiphenyl-4-yl)-3-(4-formylphenyl)acrylamide | HCID 86601892 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (E)-N-(4'-chlorobiphenyl-4-yl)-3-(4-hydroxymethylphenyl)acrylamide | HCID 68819611 | — |
反応手順
A solution of 4.4 g (12.16 mmol) of (E)-N-(4′-chlorobiphenyl-4-yl)-3-(4-formylphenyl)acrylamide in 200 mL of THF is adjusted with glacial acetic acid to a pH of three, combined with 8.14 g (36.48 mmol) of sodium triacetoxyborohydride, and stirred for 18 hours at ambient temperature. Then the reaction mixture is poured into water and the precipitate is filtered off. The filtrate is extracted with ethyl acetate, washed with water, and dried over sodium sulfate. The solvent is removed and the residue is combined with the solid which has been filtered off. The purification is carried out by column chromatography on silica gel (eluant: dichloromethane/ethanol/ammonia (30:1:0.1)). Yield: 3.2 g (72.4% of theory); C22H18ClNO2 (M=363.84); calc.: molecular ion peak (M+H)+: 364/366; found: molecular ion peak (M+H)+: 364/366; Rf value: 0.2 (silica gel, dichloromethane/ethanol (20:1)).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07592373B2 |
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| 出典データセット | uspto-grants-2009_09 |
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| ORD ID | ord-da7c9d8be14042e593bb3fd5d9ae238a |
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| 出典メモ | uspto-grants-2009_09 |
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