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Imidazole → 4-((Tert-butyldimethylsilyl)oxy)-2-fluorobenzonitrile

HRID 1873941
ノート
印刷プレビュー

反応式

HRID 1873941 の反応式
[F:1][C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].N1C=CN=C1.[CH3:16][C:17]([Si:20](Cl)([CH3:22])[CH3:21])([CH3:19])[CH3:18]>CN(C=O)C>[Si:20]([O:10][C:8]1[CH:7]=[CH:6][C:3]([C:4]#[N:5])=[C:2]([F:1])[CH:9]=1)([C:17]([CH3:19])([CH3:18])[CH3:16])([CH3:22])[CH3:21]
参加物反応条件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 27346752-Fluoro-4-hydroxybenzonitrile

生成物 1

HCID 593707824-((Tert-butyldimethylsilyl)oxy)-2-fluorobenzonitrile収率 73%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
0 °C

実験手順

2-Fluoro-4-hydroxybenzonitrile (30.1 g; manufactured by Wako Pure Chemical Industries, Ltd.) and imidazole (18.3 g; manufactured by Tokyo Chemical Industry Co., Ltd.) were dissolved in dehydrated DMF (436 mL; manufactured by Kanto Chemical Co., Inc.). After cooling to 0° C., TBDMSCl (48.3 g; manufactured by Tokyo Chemical Industry, Co., Ltd.) was added and the mixture was stirred for 1 hour while warming to room temperature. Solvent contained in the reaction solution was evaporated under reduced pressure. After adding water, extraction was carried out twice with ethyl acetate. The organic layer was washed twice with water and brine and dried over anhydrous sodium sulfate. After the solvent was evaporated under reduced pressure, purification was carried out with column chromatography (“COLUMN-A”; n-hexane:ethyl acetate=100:0→94:6) to obtain the title compound (40.3 g).

後処理

  1. temperaturewhile warming to room temperature
  2. customwas evaporated under reduced pressure
  3. additionAfter adding
  4. extractionwater, extraction
  5. washThe organic layer was washed twice with water and brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. customAfter the solvent was evaporated under reduced pressure, purification

出典と根拠

ORDレコード
ord-e885c661ccc449c48c8ee1ca1fa19b62
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08304443B2

反応ノート

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