反応式
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:20]=[CH:19][C:18]([C:21]([O:23][CH2:24][C@@H:25]([CH3:28])[CH2:26][CH3:27])=[O:22])=[CH:17][CH:16]=2)=[CH:11][CH:10]=1)C1C=CC=CC=1>[Pd].C(OCC)(=O)C>[OH:8][C:9]1[CH:10]=[CH:11][C:12]([C:15]2[CH:20]=[CH:19][C:18]([C:21]([O:23][CH2:24][C@@H:25]([CH3:28])[CH2:26][CH3:27])=[O:22])=[CH:17][CH:16]=2)=[CH:13][CH:14]=1参加物
実験手順
In a 125-ml Parr bomb equipped with a magnetic stirrer were placed 960 mg (S)-2-methyl-1-butyl 4-benzyloxy-4'-biphenylcarboxylate, 200 mg 5% palladium on carbon, and 50 ml ethyl acetate. The bomb was purged with argon and pressurized with 500 psi hydrogen. After stirring at room temperature for one day, thin layer chromatographic analysis showed that considerable starting material remained. An additional 200 mg 5% palladium on carbon was carefully added, and the bomb was re-pressurized with 500 psi hydrogen. After stirring for one more day, TLC analysis showed that the reaction was complete. The reaction mixture was filtered through Celite and the solids were washed thoroughly with ethyl acetate. Evaporation of the solvent yielded white crystals which were recrystallized from hexanes at low temperature to yield 0.62 g (85%) of product, mp 111.5°14 113° C., whose structure was confirmed by infrared, nuclear magnetic resonance, and mass spectral analyses, as follows. ##STR28##
後処理
- customIn a 125-ml Parr bomb equipped with a magnetic stirrer
- customThe bomb was purged with argon
- additionAn additional 200 mg 5% palladium on carbon was carefully added
- stirringAfter stirring for one more day, TLC analysis
- filtrationThe reaction mixture was filtered through Celite
- washthe solids were washed thoroughly with ethyl acetate
- customEvaporation of the solvent
- customyielded white crystals which
- customwere recrystallized from hexanes at low temperature
出典と根拠
- ORDレコード
- ord-1cc1ec1565934424bcfbd4acd35f9bf5
- 出典データセット
- uspto-grants-1989_08
- 特許番号
- US04857227
関連ノート
読み込み中…