Bromoacetonitrile → HCID 9880293, 화합물
반응식
[H-].[Na+].[Cl:3][C:4]1[CH:5]=[C:6]([CH:17]=[C:18]([Cl:20])[CH:19]=1)[O:7][C:8]1[C:9]([CH2:15][CH3:16])=[N:10][NH:11][C:12]=1[CH2:13][CH3:14].[H][H].Br[CH2:24][C:25]#[N:26]>CN(C)C=O>[Cl:3][C:4]1[CH:5]=[C:6]([CH:17]=[C:18]([Cl:20])[CH:19]=1)[O:7][C:8]1[C:12]([CH2:13][CH3:14])=[N:11][N:10]([CH2:24][C:25]#[N:26])[C:9]=1[CH2:15][CH3:16]참가 물질
실험 절차
Sodium hydride (60% dispersion in oil, 470 mg, 11.8 mmol) was added to a stirred solution of 4-(3,5-dichlorophenoxy)-3,5-diethyl-1H-pyrazole (3 g, 10.5 mmol, Example 3) in dry N,N-dimethylformamide (20 ml) at 0° C. under nitrogen. The mixture was stirred for 5 minutes during which time hydrogen was evolved and then bromoacetonitrile (0.81 ml, 11.6 mmol) was added. The yellow solution turned dark brown and a precipitate formed. Further dry N,N-dimethylformamide (5 ml) was added to aid dissolution and after 45 minutes the reaction mixture was quenched by the addition of water (1 ml). The mixture was partitioned between water (150 ml) and diethyl ether (2×150 ml). The combined organic layers were washed with water (50 ml) and brine (100 ml), dried over magnesium sulphate and concentrated under reduced pressure. The crude product was purified by flash chromatography on silica gel eluting with dichloromethane to provide the title compound (3.2 g) as a yellow powder, m.p. 70-72° C.
후처리
- customa precipitate formed
- customwas quenched by the addition of water (1 ml)
- customThe mixture was partitioned between water (150 ml) and diethyl ether (2×150 ml)
- washThe combined organic layers were washed with water (50 ml) and brine (100 ml)
- dry with materialdried over magnesium sulphate
- concentrationconcentrated under reduced pressure
- customThe crude product was purified by flash chromatography on silica gel eluting with dichloromethane
출처 및 근거
- ORD 기록
- ord-447a7349880949438751c2c67510ea88
- 출처 데이터셋
- uspto-grants-2011_11
- 특허 번호
- US08063044B2
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