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

HRID 2243291
ノート
印刷プレビュー

反応式

HRID 2243291 の反応式
[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]
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 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒
HCID 21867204
Cyclohexane ethylacetate
溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-9aef2b2a18e3448c8b58cc3269cfdd0f
出典データセット
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07674825B2

反応ノート

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