関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Borane | HCID 6331 | — |
| 反応物 | N-{[4-(Trifluoromethoxy)phenyl]methyl}acetamide | HCID 44542707 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Benzenemethanamine, N-ethyl-4-(trifluoromethoxy)- | HCID 20117720 | 21% |
反応手順
N-[4-(Trifluoromethoxy)benzyl]acetamide (10.4 g, 44.6 mmol) was dissolved in THF (100 mL) and cooled to −10° C. Borane (56 mL of a 2 M solution of the dimethylsulfide complex in diethyl ether) was added and the reaction mixture was stirred at −10° C. for 15 minuters and was then allowed to warm to room temperature. The reaction mixture was refluxed overnight and was then allowed to cool to room temperature. The reaction was quenched by careful addition of 10% HCl (30 mL) at 0° C. and the mixture was stirred at room temperature overnight and then concentrated in, vacuo. The residue was taken up in water (200 mL) and diethyl ether (200 mL) and the phases were separated. Concentration in vacuo of the diethyl ether phase afforded 1.9 g (21%) of the title compound as a colourless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07462644B2 |
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| 出典データセット | uspto-grants-2008_12 |
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| ORD ID | ord-1a2021ab17924aba91c7657899c5d881 |
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| 出典メモ | uspto-grants-2008_12 |
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