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Methyl acetoacetate → 6-Methyl-2-trifluoromethylpyrimidin-4-ol

HRID 1426359
ノート
印刷プレビュー

反応式

HRID 1426359 の反応式
[F:1][C:2]([F:7])([F:6])[C:3](=[NH:5])[NH2:4].O=[C:9]([CH3:15])[CH2:10][C:11](OC)=[O:12].C[O-].[Na+]>CO>[CH3:15][C:9]1[N:4]=[C:3]([C:2]([F:7])([F:6])[F:1])[NH:5][C:11](=[O:12])[CH: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

5

反応物 3

HCID 7757Methyl acetoacetateHCID 2776882TrifluoroacetamidineHCID 10942334Sodium Methoxide

生成物 1

HCID 1354086166-Methyl-2-trifluoromethylpyrimidin-4-ol

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 2,2,2-trifluoroethanimidamide (3.02 g, 22.9 mmol) and 3-oxobutanoic acid, methyl ester (2.60 mL, 24.0 mmol) in methanol (25 mL) was added 25 wt % sodium methoxide (10.5 mL, 45.8 mmol). The reaction solution was stirred at room temperature overnight. The solvent was removed in vacuo and diluted with ethyl acetate and 5M HCl. The aqueous layer was extracted with ethyl acetate once. The organic solutions were washed with brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography on a silica gel column to give the desired product as white solid.

後処理

  1. customThe solvent was removed in vacuo
  2. additiondiluted with ethyl acetate and 5M HCl
  3. extractionThe aqueous layer was extracted with ethyl acetate once
  4. washThe organic solutions were washed with brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified by flash chromatography on a silica gel column

出典と根拠

ORDレコード
ord-9e17236e3edd4a4d8bda801d283cc8b7
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08933085B2

反応ノート

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