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Imidazole → Benzaldehyde, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-

HRID 2243291
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HRID 2243291 반응식
[Si:1](Cl)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[CH:9](=[O:17])[C:10]1[C:11](=[CH:13][CH:14]=[CH:15][CH:16]=1)[OH:12].N1C=CN=C1.[OH-].[Na+]>CN(C=O)C.C1CCCCC1.CC(=O)OCC>[Si:1]([O:12][C:11]1[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=1[CH:9]=[O:17])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]
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참가 물질

7

반응물 4

HCID 795ImidazoleHCID 6998SalicylaldehydeHCID 14798Sodium HydroxideHCID 28928tert-Butyldimethylsilyl chloride

생성물 1

HCID 10900635Benzaldehyde, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-

시약·촉매·용매 2

HCID 6228Dimethylformamide용매
HCID 21867204
Cyclohexane ethylacetate
용매

실험 절차

13.58 g (90.07 mmol) of t-butyidimethylsilyl chloride (TBDMSCl) were added to a solution of 10.00 g (81.89 mmol) of salicylaldehyde and 6.13 g (90.07 mmol) of imidazole in 82 ml of DMF. The mixture was stirred at room temperature and the reaction was monitored by thin-layer chromatography (cyclohexane/EA 10:1). 1 N NaOH was added, and the mixture was extracted with petroleum ether. The combined organic phases were dried over Na2SO4, the solvent was removed and the product was purified chromatographically (silica gel, cyclohexane/EA 10:1). This gave 16.94 g (87.5%) of a clear liquid.

후처리

  1. extractionthe mixture was extracted with petroleum ether
  2. dry with materialThe combined organic phases were dried over Na2SO4
  3. customthe solvent was removed
  4. customthe product was purified chromatographically (silica gel, cyclohexane/EA 10:1)

출처 및 근거

ORD 기록
ord-9aef2b2a18e3448c8b58cc3269cfdd0f
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07674825B2

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