関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | 2,2-Dimethyl-1,3-propanediamine | HCID 81770 | — |
| 反応物 | 2-Chloro-2-methyl-3-nitrosobutane | HCID 10866386 | — |
| 生成物 | N-(3-Amino-2,2-dimethylpropyl)-1-amino-1,1-dimethyl-2-butanone oxime | HCID 87946981 | — |
反応手順
To a solution of 2,2-dimethyl-1,3-propane diamine (69 g, 0.75 mole) in dry methanol (100 mL), 3-chloro-3-methyl-2-nitrosobutane (20.55 g, 0.15 mole, Example 1) was added in portions at 0° C. over a period of 2 hours. The reaction mixture was then stirred at room temperature for 20 hours. The solvent was removed under reduced pressure to give a paste. Water (50 mL) was added, and the solution was cooled in an ice bath. The solution was filtered and the filtrate was adjusted to pH 10-11 by the addition of sodium hydroxide. The solution was cooled again and filtered. The filtrate was concentrated under reduced pressure to a paste and then extracted with ether repeatedly (10×50 mL). The combined ether solution was concentrated to give an oil which was recrystallized twice from petroleum ether to yield the title A compound as a colorless crystalline solid (20.0 g), m.p. 58-60° C. 1H NMR [CDCl3]: δ 0.85 (s, 6H, C-Me2), 1.28 (s, 6H, N—CMe2), 1.9 (s, 3H, N═CMe), 2.2 (s, 2H, NCH2) and 2.6 (s, 2H, N—CH2).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06958141B2 |
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| 出典データセット | uspto-grants-2005_10 |
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| ORD ID | ord-000200069bf6430a92a535f513fc7b6f |
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| 出典メモ | uspto-grants-2005_10 |
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