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2,5-Difluorobenzaldehyde → HCID 23114720, 화합물

HRID 2080369
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HRID 2080369 반응식
C([Li])CCC.[Si:6]([O:23][CH2:24][C:25]1[CH:26]=[N:27][CH:28]=[C:29]([F:31])[CH:30]=1)([C:19]([CH3:22])([CH3:21])[CH3:20])([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[F:32][C:33]1[CH:40]=[CH:39][C:38]([F:41])=[CH:37][C:34]=1[CH:35]=[O:36].C(=O)(O)[O-].[Na+]>CCCCCC.O.C(OCC)C>[Si:6]([O:23][CH2:24][C:25]1[CH:30]=[C:29]([F:31])[C:28]([CH:35]([C:34]2[CH:37]=[C:38]([F:41])[CH:39]=[CH:40][C:33]=2[F:32])[OH:36])=[N:27][CH:26]=1)([C:19]([CH3:21])([CH3:22])[CH3:20])([C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
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참가 물질

8

반응물 4

HCID 1376632,5-DifluorobenzaldehydeHCID 516892Sodium BicarbonateHCID 231147533-({[tert-Butyl(diphenyl)silyl]oxy}methyl)-5-fluoropyridineHCID 178418339Butyllithium

생성물 1

HCID 23114720HCID 23114720, 화합물수율 79%

시약·촉매·용매 3

HCID 962
Water
용매
HCID 3283Diethyl Ether용매2회
HCID 8058Hexane용매2회

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온도
-20 °C

실험 절차

At −78° C., a hexane solution (30.0 ml, 46.8 mmol) of n-butyl lithium and N,N,N′N′-tetramethylethylenediamine (7.06 ml, 46.8 mmol) were added sequentially to diethyl ether (250 ml). After stirring at −20° C. for 30 minutes, the reaction mixture was cooled to −78° C., and a diethyl ether (50 ml) solution of 3-(t-butyldiphenylsilyloxymethyl)-5-fluoropyridine (15.5 g, 42.5 mmol) was added thereto. The resulting mixture was stirred at the same temperature for 30 minutes. To the reaction mixture was added 2,5-difluorobenzaldehyde (6.04 g, 42.5 mmol). The resulting mixture was stirred for 2 hours. Water and then, a saturated aqueous solution of sodium bicarbonate were added to the reaction mixture. The resulting mixture was extracted with diethyl ether. The organic layer was dried over anhydrous sodium sulfate and then, filtered. The filtrate was concentrated under reduced pressure. The residue thus obtained was subjected to flash silica gel chromatography. The fraction obtained from the hexane:ethyl acetate=9:1 eluate was concentrated under reduced pressure to give the title compound (17.0 g, 33.5 mmol, 79%) as a colorless oil.

후처리

  1. temperaturethe reaction mixture was cooled to −78° C.
  2. stirringThe resulting mixture was stirred at the same temperature for 30 minutes
  3. stirringThe resulting mixture was stirred for 2 hours
  4. extractionThe resulting mixture was extracted with diethyl ether
  5. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated under reduced pressure
  8. customThe residue thus obtained
  9. concentrationethyl acetate=9:1 eluate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-5af5e15fca2e49a9b291d46987c3d020
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932271B2

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