Hydrochloric Acid → 2-Fluoro-4-hydroxybenzoic Acid

HRID 39630

反応式

HRID 39630 の反応式
[F:1][C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[C:4]#N.[OH-:11].[Na+].Cl.[OH2:14]>>[F:1][C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[C:4]([OH:14])=[O:11]

参加物

5

実験手順

To a stirred solution of 2-fluoro-4-hydroxybenzonitrile (20.00 g, 145.9 mmol) in 160 mL of water, was added 50% aqueous sodium hydroxide (40.00 g, 500.0 mmol). The mixture was heated to reflux for 4 hours, cooled to room temperature, poured into iced concentrated hydrochloric acid, and extracted with ether. The product was extracted into saturated aqueous sodium bicarbonate and the ether layer discarded. This aqueous extract was acidified with concentrated hydrochloric acid and extracted with ether. The organic extract was dried over magnesium sulfate, filtered, and evaporated to give a white solid (22.90 g) of 2-fluoro-4-hydroxybenzoic acid in 100% yield. 1H NMR (300 MHz, CD3COCD3) δ (ppm): 9.80 (b, 1H), 7.87 (t, 1H), 6.77 (dd, 1H), 6.66 (dd, 1H). 19F-NMR (300 MHz, CD3COCD3) δ (ppm): −108.13 (s, decoupled). 2-Fluoro-4-hydroxybenzonitrile: 1H-NMR (300 MHz, CD3COCD3) δ (ppm): 7.61 (t, 1H), 6.81 (m, 2H), 5.80 (b, 1H). 19F-NMR (300 MHz, CD3COCD3) δ (ppm): −108.82 (s, decoupled)

後処理

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 4 hours
  3. extractionextracted with ether
  4. extractionThe product was extracted into saturated aqueous sodium bicarbonate
  5. extractionThis aqueous extract
  6. extractionextracted with ether
  7. extractionThe organic extract
  8. dry with materialwas dried over magnesium sulfate
  9. filtrationfiltered
  10. customevaporated

出典と根拠

ORDレコード
ord-cf0a1a757f60452a84e35dfbc236a1c7
出典データセット
uspto-grants-2013_09
特許番号
US08524948B2

関連ノート

読み込み中…