반응식
[CH2:1]([OH:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].N1C=CC=CC=1.[N+:22]([C:25]1[CH:33]=[CH:32][C:28]([C:29](Cl)=[O:30])=[CH:27][CH:26]=1)([O-:24])=[O:23]>ClCCl>[N+:22]([C:25]1[CH:26]=[CH:27][C:28]([C:29]([O:15][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])=[O:30])=[CH:32][CH:33]=1)([O-:24])=[O:23]참가 물질
반응 조건
- 온도
- 30 °C
실험 절차
Under a nitrogen atmosphere, a mixture of 1-tetradecanol (96.3 grams, 449 mmol), pyridine (40 milliliters), and dichloromethane (1000 milliliters) was heated to 30° C. 4-Nitrobenzoyl chloride (100 grams, 539 mmol) was added in portions over a twenty minute period. The reaction mixture was heated to reflux for sixteen hours. The reaction mixture was washed with water (2×500 milliliters). The organic layer was concentrated under reduced pressure to a yellow solid. 1000 milliliters of hexane was added and the mixture was heated to reflux. The mixture was cooled and filtered. The filtrate was concentrated to yield a yellow solid. The yellow solid was recrystallized twice from ethanol to obtain 77.0 grams of tetradecyl 4-nitrobenzoate as yellow crystals.
후처리
- temperatureThe reaction mixture was heated
- temperatureto reflux for sixteen hours
- washThe reaction mixture was washed with water (2×500 milliliters)
- concentrationThe organic layer was concentrated under reduced pressure to a yellow solid
- addition1000 milliliters of hexane was added
- temperaturethe mixture was heated to reflux
- temperatureThe mixture was cooled
- filtrationfiltered
- concentrationThe filtrate was concentrated
- customto yield a yellow solid
- customThe yellow solid was recrystallized twice from ethanol
출처 및 근거
- ORD 기록
- ord-b35a550697104ceb8fa76ba10f219eba
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08529671B2
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