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Methanol → 3,3,3-Trifluoro-2-oxopropanoic acid

HRID 1466734
ノート
印刷プレビュー

反応式

HRID 1466734 の反応式
[F:1][C:2]([F:11])([F:10])[C:3](=[O:9])[C:4]([O:6]CC)=[O:5].[OH-].[Na+].CO>C(O)C.O>[F:1][C:2]([F:11])([F:10])[C:3](=[O:9])[C:4]([OH:6])=[O:5]
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 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 2737239Ethyl 3,3,3-trifluoro-2-oxopropanoate

生成物 1

HCID 51777643,3,3-Trifluoro-2-oxopropanoic acid収率 99%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

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

To a solution of ethyl 3,3,3-trifluoro-2-oxopropanoate (5 g, 29.36 mmol) in ethanol (30 ml) was slowly added aqueous sodium hydroxide ((2.35 g, 58.72 mmol, dissolved in water (30 ml)), and stirred for 20 h at room temperature until the starting material was consumed. The reaction mixture was concentrated and the resulting white solid was dissolved in water (100 ml). The aqueous layer was extracted by ethyl acetate (50 ml×2), and then the aqueous layer was adjusted PH to 1˜2 with concentrated HCl, and concentrated to give a white solid. The solid was added to methanol (200 ml) and stirred for overnight, filtered, and the filtrate was concentrated and dried to give the crude product (4.13 g, 99%) as a white solid, used in next step without further purification.

後処理

  1. customwas consumed
  2. concentrationThe reaction mixture was concentrated
  3. dissolutionthe resulting white solid was dissolved in water (100 ml)
  4. extractionThe aqueous layer was extracted by ethyl acetate (50 ml×2)
  5. concentrationconcentrated
  6. customto give a white solid
  7. stirringstirred for overnight
  8. filtrationfiltered
  9. concentrationthe filtrate was concentrated
  10. customdried

出典と根拠

ORDレコード
ord-27f5700531104a47b23d5f85784dd2b2
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08999985B2

反応ノート

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