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

HRID 46223
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HRID 46223 반응식
[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
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참가 물질

7

반응물 3

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

생성물 1

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

시약·촉매·용매 3

HCID 142844-(Dimethylamino)pyridine촉매
HCID 6228
Dimethylformamide
용매
HCID 25517Ammonium Chloride용매

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-3270066dc9494738a1fed70eb9f13b4f
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08541380B2

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