Water → 6-fluoro-4-oxo-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid

HRID 649531ノート

反応式

HRID 649531 の反応式
[F:1][C:2]1[CH:3]=[CH:4][C:5]2OC(C#N)[CH2:8][C:7](=[O:13])[C:6]=2[CH:14]=1.[OH2:15].[C:16]([O:19]CC)(=[O:18])[CH3:17]>Cl>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:15][CH:17]([C:16]([OH:19])=[O:18])[CH2:8][C:7](=[O:13])[C:6]=2[CH:14]=1

参加物

5

実験手順

A solution of 6-fluoro-3,4-dihydro-4-oxo-2H-1-benzopyran-2-carbonitrile (78.3 g, 0.41 mol)(obtained through the process as described in said Item (c) in 760 ml of concentrated hydrochloric acid was heated at reflux temperature for 50 minutes. After cooling the reaction solution, 700 ml of water and 1 liter of ethyl acetate were added to carry out an extraction. Resulting organic layer was evaporated in vacuo to dryness. To the residue, 700 ml of saturated sodium biscarbonate was added and stirred for 30 minutes. The aqueous basic solution was washed with 500 ml of ethyl acetate, acidified with 6N-hydrochloric acid and extracted with 1 liter of ethyl acetate. The organic layer was washed with water, dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to give 76.9 g (89.3%) of the desired compound.

後処理

  1. temperaturewas heated
  2. temperatureat reflux temperature for 50 minutes
  3. additionwere added
  4. extractionan extraction
  5. customResulting organic layer was evaporated in vacuo to dryness
  6. additionTo the residue, 700 ml of saturated sodium biscarbonate was added
  7. washThe aqueous basic solution was washed with 500 ml of ethyl acetate
  8. extractionextracted with 1 liter of ethyl acetate
  9. washThe organic layer was washed with water
  10. dry with materialdried over anhydrous sodium sulfate
  11. filtrationfiltered
  12. customevaporated in vacuo

出典と根拠

ORDレコード
ord-df0e94c0541241cabf74efc9995856ad
出典データセット
uspto-grants-1988_04
特許番号
US04740517

反応ノート

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