Dibromodifluoromethane → 4-Bromo-4,4-difluorobutanoic acid

HRID 2399725ノート

反応式

HRID 2399725 の反応式
[C:1]([OH:5])(=[O:4])[CH:2]=[CH2:3].S(S([O-])=O)([O-])=O.[Na+].[Na+].C(=O)(O)[O-].[Na+].[Br:19][C:20](Br)([F:22])[F:21]>C(OCC)(=O)C.O.C(#N)C>[Br:19][C:20]([F:22])([F:21])[CH2:3][CH2:2][C:1]([OH:5])=[O:4]

参加物

8

実験手順

To a stirred solution of acrylic acid (1.44 g) and acetonitrile (80 cm3) was added sodium dithionite (4.18 g), sodium bicarbonate (2.01 g), water (20 cm3) and finally dibromodifluoromethane (5 cm3). The biphasic mixture was stirred at the ambient temperature with the inorganic salts gradually dissolving. Gc analysis after 4 hrs indicated complete consumption of acrylic acid. The aqueous phase was saturated with solid sodium chloride. The organic phase was separated, dried (MgSO4), filtered and evaporated under reduced pressure to give a pale yellow oil with a small amount of a white solid. This mixture was taken up in ethyl acetate, filtered and evaporated under reduced pressure to give a pale yellow oil (2.54 g). 1H NMR (DMSO): δ2.65(2H,m); 2.45(2H, t).

後処理

  1. dissolutiongradually dissolving
  2. customconsumption of acrylic acid
  3. customThe organic phase was separated
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. customevaporated under reduced pressure
  7. customto give a pale yellow oil with a small amount of a white solid
  8. filtrationfiltered
  9. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-26284fce89974f5584123fe512529bbb
出典データセット
uspto-grants-1995_09
特許番号
US05451594

反応ノート

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