Benzyl Alcohol → 4-(Benzyloxy)-2-bromonicotinonitrile
반응식
[H-].[Na+].[CH2:3]([OH:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[Br:11][C:12]1[N:19]=[CH:18][CH:17]=[C:16](Br)[C:13]=1[C:14]#[N:15]>CN(C=O)C>[CH2:3]([O:10][C:16]1[C:13]([C:14]#[N:15])=[C:12]([Br:11])[N:19]=[CH:18][CH:17]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
To a suspension of NaH (1.756 g, 45.818 mmol, mineral oil 60%) in DMF (200 ml) cooled at 0° C., was added benzyl alcohol (4.542 g, 42 mmol). The resulting mixture was stirred for 5 min. Then, intermediate compound D1 (10 g, 38.18 mmol) was added. The resulting reaction mixture was gradually warmed to r.t. and stirred for 1 h, then quenched with NH4Cl (aqueous sat. solution) and diluted with H2O. The resulting mixture was extracted with Et2O. The organic layer was separated, dried (Na2SO4) and concentrated in vacuo. The crude product was purified by column chromatography (silica gel; DCM/7M solution of NH3 in MeOH up to 1% as eluent). The desired fractions were collected and concentrated in vacuo to yield intermediate compound D2 (9.2 g, 83%).
후처리
- customThe resulting reaction mixture
- temperaturewas gradually warmed to r.t.
- stirringstirred for 1 h
- customquenched with NH4Cl (aqueous sat. solution)
- additiondiluted with H2O
- extractionThe resulting mixture was extracted with Et2O
- customThe organic layer was separated
- dry with materialdried (Na2SO4)
- concentrationconcentrated in vacuo
- customThe crude product was purified by column chromatography (silica gel; DCM/7M solution of NH3 in MeOH up to 1% as eluent)
- customThe desired fractions were collected
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-a31f24d3298e4d7087c3468086ffbba5
- 출처 데이터셋
- uspto-grants-2015_07
- 특허 번호
- US09085577B2
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