Anisole → (3R,4R)-4-Methyl-5-oxopyrrolidine-3-carboxylic Acid

HRID 83486ノート

反応式

HRID 83486 の反応式
COC1C=C(OC)C=CC=1C[N:6]1[C:10](=[O:11])[C@H:9]([CH3:12])[C@@H:8]([C:13]([OH:15])=[O:14])[CH2:7]1.C1(OC)C=CC=CC=1>FC(F)(F)C(O)=O>[CH3:12][C@H:9]1[C:10](=[O:11])[NH:6][CH2:7][C@@H:8]1[C:13]([OH:15])=[O:14]

参加物

4

反応条件

温度
80 °C

実験手順

To a crude product of (3R,4R)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylic acid (8.11 g) were added anisole (3.76 ml) and trifluoroacetic acid (40 ml), and the mixture was stirred at 80° C. for 5 hours. This reaction solution was cooled to room temperature, and concentrated under reduced pressure. To the resulting residue was added diisopropyl ether, and the mixture was stirred. The insoluble substance was collected by filtration, and dried under reduced pressure to give a crude product of the titled compound (2.23 g). To the resulting solid was added ethanol (8 ml), and the mixture was heated at reflux to dissolve, and then the solution was stirred at room temperature. A solid precipitated from the mixed solution was collected by filtration, washed with a small amount of cooled ethanol, and dried under reduced pressure to give the titled compound (1.36 g).

後処理

  1. temperatureThis reaction solution was cooled to room temperature
  2. concentrationconcentrated under reduced pressure
  3. additionTo the resulting residue was added diisopropyl ether
  4. stirringthe mixture was stirred
  5. filtrationThe insoluble substance was collected by filtration
  6. customdried under reduced pressure

出典と根拠

ORDレコード
ord-f51d679885464322a7396c3ff6337fa6
出典データセット
uspto-grants-2014_09
特許番号
US08846746B2

反応ノート

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