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Water → Tert-butyl 2-acetoxyacetoacetate

HRID 130373
ノート
印刷プレビュー

反応式

HRID 130373 の反応式
[C:1]([O-:4])(=[O:3])[CH3:2].[Na+].Br[CH:7]([C:15]([CH3:17])=[O:16])[C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9].O>CN(C=O)C>[C:1]([O:4][CH:7]([C:15]([CH3:17])=[O:16])[C:8]([O:10][C:11]([CH3:12])([CH3:14])[CH3:13])=[O:9])(=[O: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

5

反応物 3

HCID 962WaterHCID 517045Sodium AcetateHCID 108899382-Bromo-3-oxobutyric acid tert-butyl ester

生成物 1

HCID 11736056Tert-butyl 2-acetoxyacetoacetate

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a suspension of sodium acetate (30.76 g, 375 mmol) in DMF (250 mL) was added dropwise tert-Butyl 2-bromo-acetoacetate (59.27 g, 250 mmol). After stirring at ambient temperature for 90 minutes, water (415 mL) was added, followed by extraction with ethyl acetate (3×325 mL). The combined organic layers were washed with water (3×325 mL) and brine (325 mL), dried over Na2SO4 and after filtration, the solvent was removed in vacuo. The resulting oil was purified by distillation (12 mbar, 128°)

後処理

  1. extractionfollowed by extraction with ethyl acetate (3×325 mL)
  2. washThe combined organic layers were washed with water (3×325 mL) and brine (325 mL)
  3. dry with materialdried over Na2SO4
  4. filtrationafter filtration
  5. customthe solvent was removed in vacuo
  6. distillationThe resulting oil was purified by distillation (12 mbar, 128°)

出典と根拠

ORDレコード
ord-015bf827b7404fa9818d5a669b2c4b44
出典データセット
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07381743B2

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