Hexane → 8-(5-Bromo-3-methylpyridin-2-yl)-1,4-dioxaspiro[4,5]decan-8-ol

HRID 1748525노트

반응식

HRID 1748525 반응식
CCCCCC.C([Li])CCC.Br[C:13]1[C:18]([CH3:19])=[CH:17][C:16]([Br:20])=[CH:15][N:14]=1.[CH2:21]1[O:31][C:24]2([CH2:29][CH2:28][C:27](=[O:30])[CH2:26][CH2:25]2)[O:23][CH2:22]1>C1(C)C=CC=CC=1.O>[Br:20][C:16]1[CH:17]=[C:18]([CH3:19])[C:13]([C:27]2([OH:30])[CH2:28][CH2:29][C:24]3([O:31][CH2:21][CH2:22][O:23]3)[CH2:25][CH2:26]2)=[N:14][CH:15]=1

참가 물질

7

실험 절차

1.6M n-Hexane solution of n-butyl lithium (100 ml) was added dropwise under nitrogen atmosphere at −78° C. to a solution of 2,5-dibromo-3-picoline (38.3 g) in toluene (300 ml), and stirred at the same temperature for two hours. Then, a solution of 1,4-cyclohexanedione monoethyleneketal (25 g) in toluene (200 ml) was added slowly dropwise, and after the addition the mixture was stirred at the same temperature for an hour. Then, the reaction solution was warmed up slowly to room temperature under stirring. After completion of the reaction, water was added and extracted with ethyl acetate. The organic layer was washed with water and saturated brine successively, dried over anhydrous sodium sulfate and concentrated. Acetonitrile and water were added to the residue and the precipitate was filtered and dried at 60° C. under air blow to give 8-(5-bromo-3-methylpyridin-2-yl)-1,4-dioxaspiro[4,5]decan-8-ol (28 g) as a light brown solid.

후처리

  1. additionafter the addition the mixture
  2. stirringwas stirred at the same temperature for an hour
  3. stirringunder stirring
  4. additionwas added
  5. extractionextracted with ethyl acetate
  6. washThe organic layer was washed with water and saturated brine successively
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated
  9. additionAcetonitrile and water were added to the residue
  10. filtrationthe precipitate was filtered
  11. customdried at 60° C. under air blow

출처 및 근거

ORD 기록
ord-5d9205395f55462b94f4c1b1eb9877e6
출처 데이터셋
uspto-grants-2015_10
특허 번호
US09150555B2

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