関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
| 反応物 | 3,4-Dichlorophenethylamine | HCID 217958 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 触媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (4-Tert-butylbenzyl)-[2-(3,4-dichloro-phenyl)-ethyl]-amine | HCID 68563688 | 102.1% |
反応手順
0.38 ml of 4-tert-butylbenzaldehyde (2.25 mmol) and 0.227 ml 2-(3,4-dichloro-phenyl)-ethylamine (1.5 mmol) were dissolved in 4.5 ml methanol at RT, and after stirring for 30 min at RT, were refluxed for 2 h. After cooling down to RT, 85 mg (2.25 mmol) sodium borohydride were added and after stirring for 5 min at RT, the reaction mixture was then refluxed for 2 h. After cooling down to RT, the reaction mixture was treated with 4 drops 1 N HCl and concentrated in vacuo. The residue was diluted with water/EtOAc. After separation of the organic phase, the aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried with magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by column chromatography (40 g silica gel; EtOAc/heptane 1:2) to give 515 mg colorless viscous oil (97%). MS (ISP) 336.2 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07745477B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-a189fa60b3d0427fa29e1260ede59189 |
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| 出典メモ | uspto-grants-2010_06 |
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