반응식
[CH3:1][C:2]([NH:5][CH2:6][Si:7]([CH3:10])([CH3:9])[CH3:8])([CH3:4])[CH3:3].[CH3:11]O.C=O.[C:15](=[O:18])([O-])[O-].[K+].[K+]>>[CH3:11][O:18][CH2:15][N:5]([CH2:6][Si:7]([CH3:10])([CH3:9])[CH3:8])[C:2]([CH3:4])([CH3:3])[CH3:1]참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
2-Methyl-N-[(trimethylsilyl)methyl]propan-2-amine (from preparation 5) (4.31 g, 27 mmol) was added to an ice-cooled mixture of methanol (1.29 mL, 31.8 mmol) and aqueous formaldehyde (37% w/v 2.49 mL, 33 mmol) over 45 minutes. The heterogeneous mixture was stirred at 0° C. for 2 hours and then solid potassium carbonate (325 mesh) (1.08 g, 13 mmol) was added and the mixture stirred for 30 minutes at 0° C. The layers were separated and the aqueous phase extracted with ethyl acetate (3×20 mL). The combined organic layers were dried over sodium sulfate, filtered, and evaporated under reduced pressure to give an 80:20 mixture of the title compound and unreacted tert-butyl[(trimethylsilyl)methyl]amine as a colourless oil (5.09 g). The mixture was used directly without further purification in preparation 2.
후처리
- temperaturecooled
- stirringthe mixture stirred for 30 minutes at 0° C
- customThe layers were separated
- extractionthe aqueous phase extracted with ethyl acetate (3×20 mL)
- dry with materialThe combined organic layers were dried over sodium sulfate
- filtrationfiltered
- customevaporated under reduced pressure
- customto give
출처 및 근거
- ORD 기록
- ord-574ce825c39f4f65bacd26f01213d8b5
- 출처 데이터셋
- uspto-grants-2010_01
- 특허 번호
- US07649002B2
연결된 노트
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