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2-(Tributylstannyl)pyridine → HCID 22235107, 화합물

HRID 1743640
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HRID 1743640 반응식
[F:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([C:9]([F:12])([F:11])[F:10])=[CH:4][C:3]=1Br.C([Sn](CCCC)(CCCC)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][N:20]=1)CCC>C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Pd]Cl>[F:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([C:9]([F:12])([F:11])[F:10])=[CH:4][C:3]=1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][N:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6077842-(Tributylstannyl)pyridineHCID 222351065-Bromo-2,4-difluorobenzotrifluoride

생성물 1

HCID 22235107HCID 22235107, 화합물

시약·촉매·용매 1

HCID 6102075Dichlorobis(triphenylphosphine)palladium촉매

실험 절차

2,4-Difluoro-5-(trifluoromethyl)bromobenzene (2.0 g, 7.7 mmol), 2-tributylstannylpyridine, and Bis(triphenylphosphine)palladium(II)chloride (0.16 g, 0.23 mmol) were added to 50 mL. xylenes and the mixture was heated to reflux for 16 hours. The reaction mixture was filtered through a silica gel plug and then purified with column chromatography to give 2-(2,4-difluoro-5-trifluoromethylphenyl)pyridine (1.4 g, 5.4 mmol). The product was confirmed by Mass Spectroscopy and 1H NMR.

후처리

  1. temperatureto reflux for 16 hours
  2. filtrationThe reaction mixture was filtered through a silica gel plug
  3. custompurified with column chromatography

출처 및 근거

ORD 기록
ord-ac858d54b27a4d21b057546ad6682c1f
출처 데이터셋
uspto-grants-2006_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07011897B2

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