Methyl p-toluenesulfonate → N-[1-(S)-[alpha-(R)-methoxybenzyl)-3-methyl-butyl]phthalimide

HRID 1935422ノート

反応式

HRID 1935422 の反応式
[OH:1][C@@H:2]([C@@H:9]([N:14]1[C:18](=[O:19])[C:17]2=[CH:20][CH:21]=[CH:22][CH:23]=[C:16]2[C:15]1=[O:24])[CH2:10][CH:11]([CH3:13])[CH3:12])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:25]1(C)C=CC(S(OC)(=O)=O)=CC=1.[H-].[Na+]>C1(C)C=CC=CC=1>[CH3:25][O:1][C@@H:2]([C@@H:9]([N:14]1[C:15](=[O:24])[C:16]2=[CH:23][CH:22]=[CH:21][CH:20]=[C:17]2[C:18]1=[O:19])[CH2:10][CH:11]([CH3:13])[CH3:12])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

参加物

5

実験手順

To a solution of N-[1-(S)-[α-(R)-hydroxybenzyl]-3-methylbutyl]phthalimide (30.4 g, 94.0 mmol.) in toluene (380 mL) were successively added methyl p-toluenesulfonate (19.2 g, 103 mmol.) and 60% sodium hydride (4.13 g, 103 mmol.). The resulting mixture was heated under reflux for 18 hours under stirring, cooled to room temperature, successively washed with water and aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by middle pressure column chromatography (n-hexane/ethyl acetate=5/1), to give N-[1-(S)-[α-(R)-methoxybenzyl]-3-methylbutyl]phthalimide as a white crystalline product (25.6 g, yield: 81%).

後処理

  1. temperatureThe resulting mixture was heated
  2. temperatureunder reflux for 18 hours
  3. washsuccessively washed with water and aqueous saturated sodium chloride solution
  4. dry with materialdried over anhydrous sodium sulfate
  5. distillationThe solvent was distilled off under reduced pressure
  6. customThe residue was purified by middle pressure column chromatography (n-hexane/ethyl acetate=5/1)

出典と根拠

ORDレコード
ord-db7dc8ea1cbe4d0b9401ea7af0ffc30e
出典データセット
uspto-grants-2002_05
特許番号
US06387908B1

反応ノート

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