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Sodium Hydroxide → 2-(Ethoxycarbonyl)-4-methylpentanoic acid

HRID 905096
ノート
印刷プレビュー

反応式

HRID 905096 の反応式
[CH2:1]([O:3][C:4]([CH:6]([CH2:12][CH:13]([CH3:15])[CH3:14])[C:7]([O:9]CC)=[O:8])=[O:5])[CH3:2].[OH-].[Na+]>C(O)C>[CH2:1]([O:3][C:4]([CH:6]([CH2:12][CH:13]([CH3:14])[CH3:15])[C:7]([OH:9])=[O:8])=[O:5])[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

4

反応物 2

HCID 14798Sodium HydroxideHCID 25047Diethyl isobutylmalonate

生成物 1

HCID 101039412-(Ethoxycarbonyl)-4-methylpentanoic acid

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Ethyl 2-(ethoxycarbonyl)-4-(methyl)pentanoate (6 g., 28 mM) was dissolved in ethanol (9 ml.) and 4 N-aqueous sodium hydroxide (7 ml.) was added. The mixture was stirred at ambient temperature for 1 hour and then evaporated. The residue was diluted with water (30 ml.) and the aqueous solution was washed with diethyl ether (3×10 ml.). The combined ethereal washings were backextracted with water (5 ml.). The combined aqueous phases were acidified to pH 3 at 0° C. with citric acid, and the resulting oil was extracted into ethyl acetate (4×20 ml.). The combined extracts were washed with water (2×20 ml.) and dried (MgSO4). The mixture was filtered and the solvent was evaporated to give 2-ethoxycarbonyl-4-methylpentanoic acid as an oil. The structure was confirmed by NMR.

後処理

  1. customevaporated
  2. additionThe residue was diluted with water (30 ml.)
  3. washthe aqueous solution was washed with diethyl ether (3×10 ml.)
  4. customwere acidified to pH 3 at 0° C. with citric acid
  5. extractionthe resulting oil was extracted into ethyl acetate (4×20 ml.)
  6. washThe combined extracts were washed with water (2×20 ml.)
  7. dry with materialdried (MgSO4)
  8. filtrationThe mixture was filtered
  9. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-43ef85ce69b44f71a46e264568aa4c2c
出典データセット
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04421744

反応ノート

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