반응식
[CH2:1]1N2CN3CN(C2)CN1C3.[C:11](O)(C(F)(F)F)=[O:12].[Br:18][C:19]1[CH:24]=[CH:23][C:22]([OH:25])=[CH:21][CH:20]=1.OS(O)(=O)=O.[OH2:31]>>[CH:1]([C:23]1[CH:24]=[C:19]([Br:18])[CH:20]=[C:21]([CH:11]=[O:12])[C:22]=1[OH:25])=[O:31]참가 물질
반응 조건
- 온도
- 120 °C
실험 절차
Hexamethylenetetramine (73.84 g, 526 mmol) was added to TFA (240 mL) with stirring. 4-Bromophenol (22.74 g, 131 mmol) was added in one portion and the solution heated in an oil bath to 120° C. and stirred under argon for 48 h. The reaction mixture was then cooled to ambient temperature. Water (160 mL) and 50% aqueous H2SO4 (80 mL) were added and the solution stirred for an additional 2 h. The reaction mixture was poured into water (1600 mL) and the resulting precipitate collected on a Büchner funnel. The precipitate was dissolved in ethyl acetate (EtOAc) and the solution was dried over MgSO4. The solution was filtered and the solvent removed on a rotary evaporator. Purification by column chromatography on silica gel (400 g) using a gradient of 15-40% ethyl acetate in hexanes resulted in a isolation of the product as a yellow solid (18.0 g, 60%).
후처리
- stirringstirred under argon for 48 h
- temperatureThe reaction mixture was then cooled to ambient temperature
- stirringthe solution stirred for an additional 2 h
- customthe resulting precipitate collected on a Büchner funnel
- dissolutionThe precipitate was dissolved in ethyl acetate (EtOAc)
- dry with materialthe solution was dried over MgSO4
- filtrationThe solution was filtered
- customthe solvent removed on a rotary evaporator
- customPurification by column chromatography on silica gel (400 g)
출처 및 근거
- ORD 기록
- ord-fe3960871dcd4b44878f683c28cc3666
- 출처 데이터셋
- uspto-grants-2009_09
- 특허 번호
- US07595368B2
연결된 노트
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