반응식
[C:1]([C:5]1[CH:6]=[C:7]([CH:14]=[C:15]([C:18]([CH3:21])([CH3:20])[CH3:19])[C:16]=1[OH:17])[CH2:8][CH2:9][C:10]([O:12][CH3:13])=[O:11])([CH3:4])([CH3:3])[CH3:2].[CH2:22](O)[CH2:23][CH2:24][CH2:25][CH2:26][CH:27](C)[CH3:28]>CC(C)[O-].[Al+3].CC(C)[O-].CC(C)[O-]>[C:1]([C:5]1[CH:6]=[C:7]([CH:14]=[C:15]([C:18]([CH3:21])([CH3:20])[CH3:19])[C:16]=1[OH:17])[CH2:8][CH2:9][C:10]([O:12][CH2:13][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])=[O:11])([CH3:3])([CH3:4])[CH3:2]참가 물질
실험 절차
Methyl 3,5-di-tert-butyl-4-hydroxyhydrocinnamate (256 g, 0.88 mole) and isooctanol (133 g, 0.91 mole) are added to a laboratory reactor equipped with the necessary auxiliary equipment. The mixture is heated to 85 C under a vacuum of 30 mmHg. After fifteen minutes, the vacuum is released and aluminum isopropoxide (1.77 g, 0.0087 mole, Rhone-Poulenc, Manalox 130) is added. The reaction mass is heated to 130 C while under a vacuum of 75 mmHg. After two hours, the reaction mass is heated to 165 C while under a vacuum of 30 mmHg for one hour. The excess isooctanol is removed by vacuum distillation at 165 C. The title compound (331 g, 97% yield) is obtained as a light yellow oil whose assay is 97% as judged by calibrated gas chromatography.
후처리
- customequipped with the necessary auxiliary equipment
- temperatureThe mixture is heated to 85 C under a vacuum of 30 mmHg
- waitAfter fifteen minutes
- temperatureThe reaction mass is heated to 130 C while under a vacuum of 75 mmHg
- temperaturethe reaction mass is heated to 165 C while under a vacuum of 30 mmHg for one hour
- customThe excess isooctanol is removed by vacuum distillation at 165 C
출처 및 근거
- ORD 기록
- ord-dfe2b5ee4f4843c1af78a0423c7fd8c6
- 출처 데이터셋
- uspto-grants-2009_05
- 특허 번호
- US07531487B2
연결된 노트
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