참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | 2,2-Dimethyl-1,3-propanediamine | HCID 81770 | — |
| 반응물 | 2-Chloro-2-methyl-3-nitrosobutane | HCID 10866386 | — |
| 생성물 | N-(3-Amino-2,2-dimethylpropyl)-1-amino-1,1-dimethyl-2-butanone oxime | HCID 87946981 | — |
반응 단계
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]: δ0.85 (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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06699458B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-74d13327b7ce47cb8e1cfe09732eb00d |
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| 출처 메모 | uspto-grants-2004_03 |
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