関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-[2-(Diethylamino)ethoxy]benzonitrile | HCID 341004 | — |
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | {4-[2-(Diethylamino)ethoxy]phenyl}methanamine | HCID 235944 | 71% |
反応手順
A 1M solution of lithium aluminium hydride (5 ml; 5 mmol) was added dropwise to a stirred solution of 1.01 g (5 mmol) of 4-(2-diethylaminoethoxy)benzonitrile in 5 ml of dry tetrahydrofuran at 0° C. The mixture was warmed to room temperature and stirred overnight. The reaction was quenched by the cautious addition of a saturated solution of 5 ml of Rochelle's salt and then evaporated. The residue was partitioned between 25 ml of diethyl ether and 25 ml of water and the organic phase was separated, dried over magnesium sulfate and evaporated. The crude product was purified by flash column chromatography on silica gel using dichloromethane/methanol/water/acetic acid (60:18:2:3) for the elution. Product-containing fractions were combined and evaporated to give 785 mg (71%) of 4-(2-diethylaminoethoxy)benzylamine as a colorless oil. [Mass spectrum (ESI) MH+ =223].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06150373 |
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| 出典データセット | uspto-grants-2000_11 |
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| ORD ID | ord-b46d2b8fa45345d09c96ddb8a2290ac2 |
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| 出典メモ | uspto-grants-2000_11 |
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