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Imidazole → ((3-Bromonaphthalen-1-yl)methoxy)triisopropylsilane

HRID 46223
ノート
印刷プレビュー

反応式

HRID 46223 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH2:12][OH:13])[C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.N1C=CN=C1.[CH3:19][CH:20]([Si:22](Cl)([CH:26]([CH3:28])[CH3:27])[CH:23]([CH3:25])[CH3:24])[CH3:21]>CN(C=O)C.CN(C1C=CN=CC=1)C.[Cl-].[NH4+]>[Br:1][C:2]1[CH:3]=[C:4]([CH2:12][O:13][Si:22]([CH:26]([CH3:28])[CH3:27])([CH:23]([CH3:25])[CH3:24])[CH:20]([CH3:21])[CH3:19])[C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 795ImidazoleHCID 139400Triisopropylsilyl chlorideHCID 12749165(3-Bromonaphthalen-1-yl)methanol

生成物 1

HCID 59463745((3-Bromonaphthalen-1-yl)methoxy)triisopropylsilane収率 96%

試薬・触媒・溶媒 3

HCID 142844-(Dimethylamino)pyridine触媒
HCID 6228
Dimethylformamide
溶媒
HCID 25517Ammonium Chloride溶媒

実験手順

To a solution of (3-bromonaphthalen-1-yl)methanol in DMF (100 mL) was added imidazole (6.4 g, 93 mmol), DMAP (0.57 g, 4.7 mmol), and TIPSCl (15 mL, 70 mmol). The resulting solution was stirred at room temperature for 12 h, diluted with a saturated ammonium chloride and extracted with EtOAc. The organic layer was washed with water then brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The crude residue was purified by column chromatography (3-10% EtOAc/hexanes) to yield the title compound (17.9 g, 96%) as a colorless oil.

後処理

  1. extractionextracted with EtOAc
  2. washThe organic layer was washed with water
  3. dry with materialbrine, dried over anhydrous MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe crude residue was purified by column chromatography (3-10% EtOAc/hexanes)

出典と根拠

ORDレコード
ord-3270066dc9494738a1fed70eb9f13b4f
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08541380B2

反応ノート

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