Acetyl chloride → 4-(Acetoxymethyl)benzoic acid

HRID 1714591ノート

反応式

HRID 1714591 の反応式
C(N([CH2:6][CH3:7])CC)C.C(Cl)(=[O:10])C.[C:12]([O:15][CH2:16][CH3:17])(=[O:14])[CH3:13].[CH2:18]1[CH2:22][O:21][CH2:20][CH2:19]1>>[C:12]([O:15][CH2:16][C:17]1[CH:7]=[CH:6][C:19]([C:20]([OH:10])=[O:21])=[CH:18][CH:22]=1)(=[O:14])[CH3:13]

参加物

5

反応条件

温度
0 °C

実験手順

Triethylamine (15.4 ml, 110.4 mmol) was added to a solution of aldehyde (2) (12.57 g, 92.4 mmol) in THF (50 ml) and cooled to 0° C. Acetyl chloride (7.91 g, 110.4 mmol) was then gradually added over 25 minutes, and the mixture was then left to stir for two hours at room temperature. After one hour, ethyl acetate (200 ml) was added and the solution washed with sodium carbonate (100 ml), HCl (17%, 50 ml) and water (100 ml) respectively. The organic layer was then dried over sodium sulfate and the solvent removed under reduced pressure to give an oil which crystallised when cooled. Re-crystallisation in methanol-hexane gave light yellow crystals.

後処理

  1. waitthe mixture was then left
  2. waitAfter one hour
  3. washthe solution washed with sodium carbonate (100 ml), HCl (17%, 50 ml) and water (100 ml) respectively
  4. dry with materialThe organic layer was then dried over sodium sulfate
  5. customthe solvent removed under reduced pressure
  6. customto give an oil which
  7. customcrystallised when
  8. temperaturecooled
  9. customRe-crystallisation in methanol-hexane gave light yellow crystals

出典と根拠

ORDレコード
ord-654e0599a6c34109b605b2e560c7281b
出典データセット
uspto-grants-2010_09
特許番号
US07795802B2

反応ノート

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