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5-Chloro-2-phenylpyridine → 5-Ethyl-2-phenylpyridine

HRID 713558
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HRID 713558 반응식
Cl[C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[N:6][CH:7]=1.[CH2:14]([Mg]Br)[CH3:15]>C1COCC1>[CH2:14]([C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[N:6][CH:7]=1)[CH3:15]
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참가 물질

4

반응물 2

HCID 27628665-Chloro-2-phenylpyridineHCID 178418443HCID 178418443, 화합물

생성물 1

HCID 5978535-Ethyl-2-phenylpyridine수율 19%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

5-Chloro-2-phenylpyridine (16 g, 84 mmol) and Ni(dppe)Cl2 (0.891 g, 1.687 mmol) were added to 300 mL of THF and the reaction mixture was degassed with nitrogen for 20 min. before being cooled to 0° C. Ethylmagnesium bromide (169 mL, 169 mmol) was added dropwise over a period of 60 min. and the reaction mixture stirred for and additional 3 h at before warming to room temperature overnight. The reaction mixture was recooled to 0° C. and quenched with 250 mL of water, extracted with EtOAc and the organic layer dried over sodium sulfate and filtered. The crude material was chromatographed on silica with 95/5 hexane/EtOAc to give 2.9 g (19%) of 5-ethyl-2-phenylpyridine as a white solid.

후처리

  1. customthe reaction mixture was degassed with nitrogen for 20 min.
  2. temperaturebefore warming to room temperature overnight
  3. customwas recooled to 0° C.
  4. customquenched with 250 mL of water
  5. extractionextracted with EtOAc
  6. dry with materialthe organic layer dried over sodium sulfate
  7. filtrationfiltered
  8. customThe crude material was chromatographed on silica with 95/5 hexane/EtOAc

출처 및 근거

ORD 기록
ord-501eb203d6c542168dea71438a871f8d
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09184397B2

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