Water → HCID 67399383, 화합물

HRID 70542

반응식

HRID 70542 반응식
C[Si](C)(C)[N-][Si](C)(C)C.[Li+].[I-].C1([P+](C2C=CC=CC=2)(C2C=CC=CC=2)[CH2:19][CH:20]2[CH2:25][CH2:24][O:23][CH2:22][CH2:21]2)C=CC=CC=1.[Cl:38][C:39]1[CH:40]=[CH:41][C:42]([CH:47]=O)=[N:43][C:44]=1[O:45][CH3:46].O>O1CCCC1>[Cl:38][C:39]1[C:44]([O:45][CH3:46])=[N:43][C:42](/[CH:47]=[CH:19]\[CH:20]2[CH2:21][CH2:22][O:23][CH2:24][CH2:25]2)=[CH:41][CH:40]=1

참가 물질

6

실험 절차

A solution of lithium hexamethyldisilazide in tetrahydrofuran (1 M, 10 mL) was added to a solution of triphenyl(tetrahydro-2H-pyran-4-ylmethyl)phosphonium iodide (5.51 g) in tetrahydrofuran (20 mL) under ice-cooling, and the mixture was stirred at room temperature for one hour. A solution of 5-chloro-6-methoxypyridine-2-carbaldehyde (1.3 g) in tetrahydrofuran (20 mL) was slowly added to the reaction solution, and the mixture was stirred at room temperature for one hour. The reaction solution was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The filtrate was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to give 3-chloro-2-methoxy-6-[(Z)-2-(tetrahydro-2H-pyran-4-yl)ethenyl]pyridine as a colorless powder (1.62 g, 60%).

후처리

  1. temperaturecooling
  2. stirringthe mixture was stirred at room temperature for one hour
  3. extractionfollowed by extraction with ethyl acetate
  4. washThe organic layer was washed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customThe solvent was then evaporated under reduced pressure
  8. customThe filtrate was purified by silica gel column chromatography (hexane:ethyl acetate=4:1)

출처 및 근거

ORD 기록
ord-5cc8e5298ab243bfb54577433be3f815
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08822503B2

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