関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methylamine | HCID 6329 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 3-Chlorobenzofuran-2-carboxaldehyde | HCID 4737020 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (3-Chloro-benzofuran-2-ylmethyl)methylamine | HCID 59277587 | 82.1% |
反応手順
To a solution of 3-chlorobenzofuran-2-carboxaldehyde (1.62 g, 8.9 mmol) in methanol (50 mL) is added N-methylamine (33% solution in ethanol, 1.11 g, 35.9 mmol) and stirred overnight at room temperature. The mixture is concentrated in vacuo, re-solvated in methanol (50 mL) and cooled in an ice bath. Sodium borohydride (407 mg, 10.8 mmol) is added in portions and the mixture stirred at room temperature for 4 h. The mixture is concentrated in vacuo, re-solvated in 1.3M sodium hydroxide solution, stirred for 20 min, extracted with ethyl acetate, dried with sodium sulfate and concentrated. Purification by column chromatography (silica, CH2Cl2/MeOH, 9/1) gave title compound (1.43 g, 82%) as a colorless oil. 1H NMR (300 MHz, DMSO-d6) δ 7.55-7.63 (m, 2H), 7.33-7.42 (m, 2H), 3.93 (s, 2H), 2.27 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08450307B2 |
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| 出典データセット | uspto-grants-2013_05 |
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| ORD ID | ord-71edb359272c4abe834da01637e39e37 |
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| 出典メモ | uspto-grants-2013_05 |
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