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Triacetoxyperiodinane → 5-Fluoro-2-methoxy-4-(2-oxoethyl)benzonitrile

HRID 1474245
ノート
印刷プレビュー

反応式

HRID 1474245 の反応式
[F:1][C:2]1[C:3]([CH2:12][CH2:13][OH:14])=[CH:4][C:5]([O:10][CH3:11])=[C:6]([CH:9]=1)[C:7]#[N:8].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>ClCCl.C([O-])(O)=O.[Na+].[O-]S([O-])(=S)=O.[Na+].[Na+]>[F:1][C:2]1[C:3]([CH2:12][CH:13]=[O:14])=[CH:4][C:5]([O:10][CH3:11])=[C:6]([CH:9]=1)[C:7]#[N:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 159087TriacetoxyperiodinaneHCID 666439605-Fluoro-4-(2-hydroxyethyl)-2-methoxybenzonitrile

生成物 1

HCID 866944585-Fluoro-2-methoxy-4-(2-oxoethyl)benzonitrile

試薬・触媒・溶媒 3

HCID 6344Dichloromethane溶媒HCID 24477Sodium Thiosulfate溶媒HCID 516892
Sodium Bicarbonate
溶媒

実験手順

To a solution of 5-fluoro-4-(2-hydroxyethyl)-2-methoxybenzonitrile (175 mg, 0.900 mmol) in Dichloromethane (4 mL) was added Dess-Martin Periodinane (0.53 g, 1.2 mmol). The solution was stirred for 2 h at ambient temperature, then was diluted with NaHCO3 (sat.) and Na2S2O3 (sat.) and stirred for 30 min. The layers were separated and the aqueous layer was extracted with dichloromethane twice. The combined organics were washed with brine, dried (MgSO4), filtered, and concentrated to provide the desired aldehyde, which was used directly without further purification.

後処理

  1. stirringstirred for 30 min
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted with dichloromethane twice
  4. washThe combined organics were washed with brine
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-052179e644934115893646a1ade386c9
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09018211B2

反応ノート

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