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2-(Dimethylamino)ethanol → 2-Methoxy-6-(tributylstannyl)pyridine

HRID 447039
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인쇄 미리보기

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HRID 447039 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]=1
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참가 물질

7

반응물 4

HCID 79022-(Dimethylamino)ethanolHCID 15096Tributyltin ChlorideHCID 742012-MethoxypyridineHCID 178418339Butyllithium

생성물 1

HCID 105248912-Methoxy-6-(tributylstannyl)pyridine

시약·촉매·용매 2

HCID 962Water용매
HCID 8058
Hexane
용매
2회

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

  1. temperaturethe reaction medium was cooled to −78° C.
  2. customThe resulting reaction mixture
  3. stirringwas stirred at −78° C. for 30 min
  4. stirringto stir at 0-5° C. for 30 min
  5. customto come to room temperature
  6. customAfter the completion of reaction (TLC monitoring)
  7. temperaturethe reaction mass was cooled to 0° C.
  8. extractionThe aqueous phase was extracted with diethyl ether (3×50 mL)
  9. dry with materialThe combined organic layers were dried over anhydrous Na2SO4
  10. customevaporated to dryness
  11. 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
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08481544B2

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