Hydrochloric Acid → 2-(4-Bromo-2,6-difluorophenyl)acetic acid

HRID 1525904ノート

反応式

HRID 1525904 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([CH2:9][C:10](N)=[O:11])=[C:4]([F:13])[CH:3]=1.[OH-:14].[Na+].Cl>C(O)C>[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([CH2:9][C:10]([OH:14])=[O:11])=[C:4]([F:13])[CH:3]=1

参加物

5

反応条件

温度
80 °C

実験手順

A suspension of 2-(4-bromo-2,6-difluorophenyl)acetamide (7.20 mmol) in ethanol (10 mL) was treated with 6N aq sodium hydroxide (90 mmol) at room temperature. The vessel was then stirred in an oil bath at 80° C. After one hour the reaction mixture had turned clear. After stirring overnight, the reaction mixture was cooled to room temperature, at which point the pH was adjusted to ˜1 with 6N aq HCl. A white precipitate formed, and the solution was concentrated to a volume of ˜10 mL, at which point it was extracted three times with ethyl acetate. The combined organic layers were washed twice with brine, dried over sodium sulfate, filtered and concentrated in vacuo to afford the title compound as a solid (837 mg, 41% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 3.60 (s, 2 H) 7.49 (d, J=6.82 Hz, 2 H) 12.82 (br. s., 1 H).

後処理

  1. stirringAfter stirring overnight
  2. temperaturethe reaction mixture was cooled to room temperature, at which point the pH
  3. customA white precipitate formed
  4. concentrationthe solution was concentrated to a volume of ˜10 mL, at which point it
  5. extractionwas extracted three times with ethyl acetate
  6. washThe combined organic layers were washed twice with brine
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-dabb8ab7bacc4c2cbb17abcc8a52ec13
出典データセット
uspto-grants-2015_07
特許番号
US09084794B2

反応ノート

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