関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Methylpiperidine | HCID 7974 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 5-Bromo-2-fluorobenzaldehyde | HCID 736327 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 5-Bromo-2-(2-methylpiperidin-1-YL)benzaldehyde | HCID 23091101 | 89% |
反応手順
To a solution of 5-bromo-2-fluorobenzaldehyde (13.20 g; 65.02 mmol) in DMSO (160 mL) and water (40 mL) were added 2-methylpiperidine (15.35 mL; 130.04 mmol) and anhydrous sodium carbonate (13.78 g; 130.04 mmol). The resulting mixture was heated at 120° C. for 16 h after which it was allowed to cool to RT. Reaction mixture was partitioned between H2O (1 L) and Et2O (2×750 mL) and the combined organic layers were washed with brine (500 mL, pH 5-6 adjusted with HCl), dried over MgSO4, filtered and dried under vacuum to give the title compound as a brown yellow oil (16.3 g, 89%). LC/MS (Method B): 282.1 (M+H)+. HPLC (Method A): Rt 2.20 min (Purity: 93.7%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08202865B2 |
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| 出典データセット | uspto-grants-2012_06 |
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| ORD ID | ord-98f3cacdfd4142f4b412f292328078fa |
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| 出典メモ | uspto-grants-2012_06 |
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