Sodium hydride → 5-(3-Cyclohexyl-propoxy)-1-(4-nitro-phenyl)-1H-tetrazole
반응식
[CH:1]1([CH2:7][CH2:8][CH2:9][OH:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[Na+].Cl[C:14]1[N:18]([C:19]2[CH:24]=[CH:23][C:22]([N+:25]([O-:27])=[O:26])=[CH:21][CH:20]=2)[N:17]=[N:16][N:15]=1>O1CCCC1>[CH:1]1([CH2:7][CH2:8][CH2:9][O:10][C:14]2[N:18]([C:19]3[CH:20]=[CH:21][C:22]([N+:25]([O-:27])=[O:26])=[CH:23][CH:24]=3)[N:17]=[N:16][N:15]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1참가 물질
실험 절차
Cyclohexylpropyl alcohol (237 mL, 1.56 mol) was added to a suspension of NaH (66.0 g, 1.65 mol) in tetrahydrofuran (1.40 L). A solution of 5-Chloro-1-(4-nitro-phenyl)-1H-tetrazole (320 g, 1.42 mol) in tetrahydrofuran (900 mL) was added dropwise over 1.5 hours. The reaction was allowed to cool to room temperature and stirred overnight. The mixture was concentrated in vacuo to a solid. The solid was dissolved in ethyl acetate, washed with saturated aqueous sodium chloride solution (2×), dried (Na2SO4), and filtered through silica gel (700 g). The red filtrate was concentrated in vacuo until product began to precipitate from solution. Hexane was added and the slurry filtered to provide a tan solid (320 g, 64%). Mp 82-88° C. (dec); 1H NMR (CDCl3, 300 MHz) δ 8.43 (d, 9.2 Hz, 2H), 8.04 (d, 9.2 Hz, 2H), 4.70 (t, 7.0 Hz, 2H), 1.96 (m, 2H), 1.75-1.64 (m, 5H), 1.39-1.13 (m, 6H), 0.97-0.87 (m, 2H); MS (CI) m/z 332 (MH+); Anal. calcd for C16H21N5O3: C, 57.99; H, 6.39; N, 21.13. Found: C, 57.80; H, 6.35; N, 21.02; Rf=0.43 (N).
후처리
- concentrationThe mixture was concentrated in vacuo to a solid
- dissolutionThe solid was dissolved in ethyl acetate
- washwashed with saturated aqueous sodium chloride solution (2×)
- dry with materialdried (Na2SO4)
- filtrationfiltered through silica gel (700 g)
- concentrationThe red filtrate was concentrated in vacuo until product
- customto precipitate from solution
- additionHexane was added
- filtrationthe slurry filtered
출처 및 근거
- ORD 기록
- ord-b10ad2b68e2e47c1826cbfdc33a87c5c
- 출처 데이터셋
- uspto-grants-2005_06
- 특허 번호
- US06903218B2
반응 노트
불러오는 중…