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Propionic anhydride → 3-(3,4-Difluorophenyl)-2-methylprop-2-enoic acid

HRID 1609630
ノート
印刷プレビュー

反応式

HRID 1609630 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[F:10])[CH:5]=O.[C:11]([O:15]C(=O)CC)(=[O:14])[CH2:12][CH3:13].C([O-])(=O)CC.[Na+]>O>[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[F:10])[CH:5]=[C:12]([CH3:13])[C:11]([OH:15])=[O:14]
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 31263Propionic anhydrideHCID 5880883,4-DifluorobenzaldehydeHCID 2723816Sodium Propionate

生成物 1

HCID 539805853-(3,4-Difluorophenyl)-2-methylprop-2-enoic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of 2.88 g. (0.02 mole) of 3,4-difluorobenzaldehyde, 3.24 g. (0.025 mole) of propionic anhydride and 0.92 g. (0.02 mole) of sodium propionate under nitrogen is heated at 135° with a magnetic stirrer for 20 hours. The reaction mixture is poured onto 50 ml. of water. A solid precipitates that dissolves when 50 ml. of saturated K2CO3 is added with stirring. The basic solution is extracted with ether (2×100 ml.). The aqueous phase is then poured into an excess of concentrated HCl and ice. The precipitated white solid is filtered and dried to give 3,4-difluoro-α-methylcinnamic acid, M.P. 122°-125°.

後処理

  1. additionA mixture of 2.88 g
  2. additionThe reaction mixture is poured onto 50 ml
  3. customA solid precipitates
  4. dissolutionthat dissolves when 50 ml
  5. additionof saturated K2CO3 is added
  6. extractionThe basic solution is extracted with ether (2×100 ml.)
  7. additionThe aqueous phase is then poured into an excess of concentrated HCl and ice
  8. filtrationThe precipitated white solid is filtered
  9. customdried

出典と根拠

ORDレコード
ord-dc2c68c0deff4e93980b52ce78da2bcb
出典データセット
uspto-grants-1995_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05401774

反応ノート

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