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Imidazole → Benzene, 1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-fluoro-5-methyl-

HRID 1020793
ノート
印刷プレビュー

反応式

HRID 1020793 の反応式
[F:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[C:6]([CH3:8])[CH:7]=1.[Si:10](Cl)([C:13]([CH3:16])([CH3:15])[CH3:14])([CH3:12])[CH3:11].N1C=CN=C1>ClCCl>[C:13]([Si:10]([O:9][C:4]1[CH:5]=[C:6]([CH3:8])[CH:7]=[C:2]([F:1])[CH:3]=1)([CH3:12])[CH3:11])([CH3:16])([CH3:15])[CH3:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 35496693-Fluoro-5-methylphenol

生成物 1

HCID 66726507Benzene, 1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-fluoro-5-methyl-収率 102.9%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 3-fluoro-5-methylphenol (19.7 g, 156 mmol) and tert-butyldimethylsilyl chloride (25.9 g, 172 mmol) in dichloromethane (250 mL) was added imidazole (12.7 g, 187 mmol) at 0° C., and the mixture was stirred at room temperature for 2 h. The mixture was washed with water and brine and dried on anhydrous sodium sulfate. The solvent was removed in vacuo, and the residue was purified by silica gel chromatography (98:2 hexane/ethyl acetate) to give tert-butyl(3-fluoro-5-methylphenoxy)dimethylsilane (38.6 g, 100%).

後処理

  1. washThe mixture was washed with water and brine
  2. dry with materialdried on anhydrous sodium sulfate
  3. customThe solvent was removed in vacuo
  4. customthe residue was purified by silica gel chromatography (98:2 hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-91ab94f0efc84d2b9889996de2634ab1
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08716478B2

反応ノート

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