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2-Chloro-2,3,3-trifluorobutanedioic acid → 2,2,3-Trifluorobutanedioic acid

HRID 1567
ノート
印刷プレビュー

反応式

HRID 1567 の反応式
Cl[C:2]([F:12])([C:9]([OH:11])=[O:10])[C:3]([F:8])([F:7])[C:4]([OH:6])=[O:5]>O1CCOCC1.[Zn]>[F:7][C:3]([F:8])([CH:2]([F:12])[C:9]([OH:11])=[O:10])[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

4

反応物 1

HCID 189170672-Chloro-2,3,3-trifluorobutanedioic acid

生成物 1

HCID 190657982,2,3-Trifluorobutanedioic acid収率 40.7%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 312751,4-Dioxane溶媒

実験手順

To a stirring solution of the chlorotrifluorosuccinic acid (part b) (24.5 g) in 200 ml dioxane was added portionwise zinc metal (85 g) and the mixture was stirred at ambient temperature for 10 hours to yield a viscous liquid which was decanted from the unreacted zinc. Most of the dioxane was evaporated in vacuo. The residue was dissolved in 100 ml H2O and a solution of 7.7 ml of concentrated H2SO4 in 25 ml of water was added. The solution was extracted with ether (3×100 ml) and dried over anhydrous MgSO4. The organic layer was stripped to yield 8.3 g (32%) of the product as a crystalline solid.

後処理

  1. customto yield a viscous liquid which
  2. customwas decanted from the unreacted zinc
  3. customMost of the dioxane was evaporated in vacuo
  4. dissolutionThe residue was dissolved in 100 ml H2O
  5. additiona solution of 7.7 ml of concentrated H2SO4 in 25 ml of water was added
  6. extractionThe solution was extracted with ether (3×100 ml)
  7. dry with materialdried over anhydrous MgSO4

出典と根拠

ORDレコード
ord-12d76bd288204ab9895441c0ad284664
出典データセット
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05726176

反応ノート

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