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Isopropyl Acetate → 2-Methoxypyrimidine-5-carboxaldehyde

HRID 657750
ノート
印刷プレビュー

反応式

HRID 657750 の反応式
S(O)(O)(=O)=O.[CH3:6][O:7][C:8](=[NH:10])[NH2:9].C[O:12][C:13](=N)N.C[NH+]([CH2:19][C:20](CN(C)C)=[CH:21][NH+](C)C)C.C(OC(C)C)(=O)C.C(=O)(O)[O-].[K+]>O>[CH3:6][O:7][C:8]1[N:9]=[CH:21][C:20]([CH:13]=[O:12])=[CH:19][N:10]=1
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 4

HCID 7915Isopropyl AcetateHCID 516893Potassium BicarbonateHCID 11357018Bis(2-methylisouronium) sulphateHCID 101612644Vinamidinium

生成物 1

HCID 31518662-Methoxypyrimidine-5-carboxaldehyde

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

To a stirred slurry of O-methylisourea hemisulfate (1.08 g, 4.13 mmol), vinamidinium salt (3.00 g, 8.26 mmol), 1-methylethyl acetate (16.0 mL, 137 mmol) was added a solution of potassium bicarbonate (1.17 g, 11.6 mmol) in water (5.0 mL) over a 10 minutes period. After completion of the addition the resulting reaction mixture was stirred at room temperature for 40 hours. The mixture was diluted with water (20 mL) and extracted with EtOAc (2×25 mL). The combined organic layers were dried over sodium sulfate and concentrated to yield a white solid.

後処理

  1. additionAfter completion of the addition
  2. customthe resulting reaction mixture
  3. extractionextracted with EtOAc (2×25 mL)
  4. dry with materialThe combined organic layers were dried over sodium sulfate
  5. concentrationconcentrated
  6. customto yield a white solid

出典と根拠

ORDレコード
ord-fe6c5ecaa1a94111831f0dae382a8cf6
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08076345B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート