반응식
CN(C)CCO.[Li]CCCC.[CH3:12][O:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=1.[CH2:20]([Sn:24](Cl)([CH2:29][CH2:30][CH2:31][CH3:32])[CH2:25][CH2:26][CH2:27][CH3:28])[CH2:21][CH2:22][CH3:23]>CCCCCC.O>[CH3:12][O:13][C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([Sn:24]([CH2:25][CH2:26][CH2:27][CH3:28])([CH2:29][CH2:30][CH2:31][CH3:32])[CH2:20][CH2:21][CH2:22][CH3:23])[N:15]=1참가 물질
반응 조건
- 온도
- 2.5 °C
실험 절차
To a solution of 2-dimethylaminoethanol (3.50 mL, 16.36 mmol) in hexane (20.0 mL, HPLC grade) cooled at −5° C. was added drop wise n-BuLi (3.60 M, 9.0 mL, 32.40 mmol) under nitrogen atmosphere. After 30 min at 0° C., 2-methoxy-pyridine (0.60 g, 5.45 mmol) in hexane (20.0 mL) was added drop wise. After stirring the reaction mixture for 1 h at 0-5° C., the reaction medium was cooled to −78° C. followed by drop wise addition of tributyl tin chloride (3.70 mL, 13.62 mmol). The resulting reaction mixture was stirred at −78° C. for 30 min and then allowed to stir at 0-5° C. for 30 min. The reaction mixture was then allowed to come to room temperature. After the completion of reaction (TLC monitoring), the reaction mass was cooled to 0° C. and water was added slowly. The aqueous phase was extracted with diethyl ether (3×50 mL). The combined organic layers were dried over anhydrous Na2SO4, and evaporated to dryness. The crude residue (1.80 g, 72%) was carried forward to the next step without further purification.
후처리
- temperaturethe reaction medium was cooled to −78° C.
- customThe resulting reaction mixture
- stirringwas stirred at −78° C. for 30 min
- stirringto stir at 0-5° C. for 30 min
- customto come to room temperature
- customAfter the completion of reaction (TLC monitoring)
- temperaturethe reaction mass was cooled to 0° C.
- extractionThe aqueous phase was extracted with diethyl ether (3×50 mL)
- dry with materialThe combined organic layers were dried over anhydrous Na2SO4
- customevaporated to dryness
- customThe crude residue (1.80 g, 72%) was carried forward to the next step without further purification
출처 및 근거
- ORD 기록
- ord-0ffbc4709d584fbbbcbb22d89f0e0312
- 출처 데이터셋
- uspto-grants-2013_07
- 특허 번호
- US08481544B2
연결된 노트
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