関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | 2-Iodo-4-nitroaniline | HCID 222629 | — |
| 反応物 | 2-((Tert-butyldimethylsilyl)oxy)acetaldehyde | HCID 4187788 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (2-(Tert-butyl-dimethyl-silanyloxy)-ethyl]-(2-iodo-4-nitro-phenyl)-amine | HCID 59129393 | 25% |
反応手順
To a solution of 2-iodo-4-nitroaniline (2.0 g, 7.6 mmol) and 2-(tert-butyldimethylsilyloxy)-acetaldehyde (3.5 g, 75% purity, 15 mmol) in methanol (30 mL) was added TFA (1.5 mL) at 0° C. The reaction mixture was stirred at this temperature for 30 min before NaCNBH3 (900 mg, 15 mmol) was added in portions. The mixture was stirred for 2 h and was then quenched with water. The resulting mixture was extracted with EtOAc (30 mL×3), the combined organic extracts were dried over anhydrous Na2SO4 and evaporated under vacuum, and the residue was purified by chromatography on silica gel (5% ethyl acetate/petroleum) to afford [2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-(2-iodo-4-nitro-phenyl)-amine (800 mg, 25%). 1H NMR (300 MHz, CDCl3) δ 8.57 (d, J=2.7 Hz, 1 H), 8.12 (dd, J=2.4, 9.0 Hz, 1 H), 6.49 (d, J=9.3 Hz, 1 H), 5.46 (br s, 1 H), 3.89 (t, J=5.4 Hz, 2 H), 3.35 (q, J=5.4 Hz, 2 H), 0.93 (s, 9 H), 0.10 (s, 6 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08415387B2 |
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| 出典データセット | uspto-grants-2013_04 |
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| ORD ID | ord-0fdb3c61171a4891b777ee6e94b078b4 |
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| 出典メモ | uspto-grants-2013_04 |
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