Water → Methyl 2-(4-formylphenyl)acetate

HRID 339939ノート

反応式

HRID 339939 の反応式
C[N+]1([O-])CC[O:5]CC1.Br[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([CH2:17][C:18]([O:20][CH3:21])=[O:19])=[CH:13][CH:12]=1.O>CC#N.C1(C)C=CC=CC=1>[CH:10]([C:11]1[CH:16]=[CH:15][C:14]([CH2:17][C:18]([O:20][CH3:21])=[O:19])=[CH:13][CH:12]=1)=[O:5]

参加物

6

実験手順

To a mixture of N-methylmorpholine-N-oxide (63.9 g, 545 mmol) in MeCN (848 g) and toluene (742 g), was added a solution of methyl [4-(bromomethyl)phenyl]acetate (53.0 g) in toluene (212 g) at 0 to 25° C. After stirring for 5 hr, water (106 g) was added to the reaction mixture. The aqueous layer was removed and remaining MeCN in the organic layer was removed under reduced pressure. The remaining toluene solution was washed with water twice (530 g×2), and concentrated under reduced pressure at a temperature below 40° C. until the weight of the solution was 233 g. An activated charcoal (3 g) was added to the solution and removed by filtration. To the solution was added 2,6-dibutyl-4-hydroxytoluene (152 mg), and concentrated under reduced pressure to give the subtitle compound. Yield 30.9 g, 79% from methyl [4-(bromomethyl)phenyl]acetate; 1H NMR (DMSO-d6) δ 9.99 (s, 1H), 7.87 (d, 2H), 7.86 (d, 2H), 3.83 (s, 2H), 3.63 (s, 3H)

後処理

  1. customThe aqueous layer was removed
  2. customwas removed under reduced pressure
  3. washThe remaining toluene solution was washed with water twice (530 g×2)
  4. concentrationconcentrated under reduced pressure at a temperature below 40° C. until the weight of the solution
  5. additionAn activated charcoal (3 g) was added to the solution
  6. customremoved by filtration
  7. additionTo the solution was added 2,6-dibutyl-4-hydroxytoluene (152 mg)
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-03484f212d3d478bbb1253f055dc89be
出典データセット
uspto-grants-2014_11
特許番号
US08895570B2

反応ノート

読み込み中…