Water → [2-Methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-acetic Acid

HRID 890447ノート

反応式

HRID 890447 の反応式
[CH3:1][C:2]1[C:7]([CH2:8][C:9]#N)=[CH:6][CH:5]=[C:4]([C:11]2[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:13][CH:12]=2)[N:3]=1.[OH-:21].[Na+].[OH2:23]>C(O)CC>[CH3:1][C:2]1[C:7]([CH2:8][C:9]([OH:23])=[O:21])=[CH:6][CH:5]=[C:4]([C:11]2[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:13][CH:12]=2)[N:3]=1

参加物

5

反応条件

温度
100 °C

実験手順

A mixture of 25 g (90 mmol) of the above prepared [2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-acetonitrile, 20 g of sodium hydroxide (500 mmol), 60 ml of water and 250 ml of propanol was stirred vigorously at 100° C. Hydrolysis was complete after 2 hours. The reaction mixture was then evaporated to dryness and the residue was dissolved in 70 ml of water; then, 60 ml of cold 8 N aqueous HCl were added and the compound was extracted with three portions of 250 ml of ethyl acetate; the combined organic phases were washed with water and brine, dried with anhydrous sodium sulfate and evaporated. 25.1 g (93.9%) of [2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-acetic acid were obtained as a pale yellow solid.

後処理

  1. additionA mixture of 25 g (90 mmol) of the
  2. customHydrolysis
  3. customThe reaction mixture was then evaporated to dryness
  4. dissolutionthe residue was dissolved in 70 ml of water
  5. additionthen, 60 ml of cold 8 N aqueous HCl were added
  6. extractionthe compound was extracted with three portions of 250 ml of ethyl acetate
  7. washthe combined organic phases were washed with water and brine
  8. dry with materialdried with anhydrous sodium sulfate
  9. customevaporated

出典と根拠

ORDレコード
ord-f3cbcf9b3ae34e158c31bed315bb61c0
出典データセット
uspto-grants-2006_02
特許番号
US06995263B2

反応ノート

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