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1-Bromononane → 2-(5-Chloro-2-(n-nonyloxy)phenyl)-1-(1h-1-imidazolyl)-2-propanol

HRID 1582621
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HRID 1582621 반응식
[OH-].[Na+].[CH2:3](Br)[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([OH:20])=[C:16]([C:21]([OH:29])([CH3:28])[CH2:22][N:23]2[CH:27]=[CH:26][N:25]=[CH:24]2)[CH:15]=1>CN(C)C=O>[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([O:20][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])=[C:16]([C:21]([OH:29])([CH3:28])[CH2:22][N:23]2[CH:27]=[CH:26][N:25]=[CH:24]2)[CH:15]=1
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참가 물질

5

반응물 3

HCID 127421-BromononaneHCID 14798Sodium HydroxideHCID 129728974-chloro-2-(1-hydroxy-2-(1H-1-imidazolyl)-1-methylethyl)phenol2회

생성물 1

HCID 99078142-(5-Chloro-2-(n-nonyloxy)phenyl)-1-(1h-1-imidazolyl)-2-propanol수율 54.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Sodium hydroxide powder (20 mg, 0.5 mmol) and n-nonyl bromide (122 mg, 0.59 mmol) were added to a solution of 4-chloro-2-(1-hydroxy-2-(1H-1-imidazolyl)-1-methylethyl)phenol [compound (2-1)] (100 mg, 0.40 mmol) in N,N-dimethylformamide (1 mL), and the mixture was stirred for 17 hours at room temperature. Ice-water was added to the resultant mixture, followed by extraction with ethyl acetate. The organic layer was washed with water and dried over magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified through silica gel column chromatography and dried under reduced pressure, to thereby yield 2-(5-chloro-2-(n-nonyloxy)phenyl)-1-(1H-1-imidazolyl)-2-propanol as a colorless oily product (81.7 mg, yield: 54.5%).

후처리

  1. extractionfollowed by extraction with ethyl acetate
  2. washThe organic layer was washed with water
  3. dry with materialdried over magnesium sulfate
  4. customThe solvent was removed under reduced pressure
  5. customThe residue was purified through silica gel column chromatography
  6. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-859e93c5465c470a8b29dca6b46c05bf
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06737434B2

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