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Trimethylsilylacetylene → 3-Bromo-5-((trimethylsilyl)ethynyl)pyridine

HRID 606803
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인쇄 미리보기

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HRID 606803 반응식
[CH3:1][Si:2]([C:5]#[CH:6])([CH3:4])[CH3:3].[Br:7][C:8]1[CH:9]=[N:10][CH:11]=[C:12](I)[CH:13]=1>C(N(CC)CC)C.C(#N)C.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[Br:7][C:8]1[CH:9]=[N:10][CH:11]=[C:12]([C:6]#[C:5][Si:2]([CH3:4])([CH3:3])[CH3:1])[CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 66111TrimethylsilylacetyleneHCID 8204093-Bromo-5-iodopyridine

생성물 1

HCID 665244243-Bromo-5-((trimethylsilyl)ethynyl)pyridine수율 99%

시약·촉매·용매 3

HCID 178418476HCID 178418476, 화합물촉매HCID 6342Acetonitrile용매HCID 8471
Triethylamine
용매

실험 절차

Add trimethylsilylacetylene (54.6 mL, 389.4 mmol) to a stirred mixture of 3-bromo-5-iodopyridine (100 g, 354 mmol) in triethylamine (800 mL) and acetonitrile (800 mL). Purge the system with nitrogen and add bis(triphenylphosphine)palladium(II) dichloride (3.54 mmol, 2.48 g) and stir for 16 h. Concentrate and suspend the residue in 1800 mL of hexanes. Stir for 2 h, filter and concentrate to give the title compound as a brown solid (92g, 99%).

후처리

  1. customPurge the system with nitrogen
  2. concentrationConcentrate
  3. stirringStir for 2 h
  4. filtrationfilter
  5. concentrationconcentrate

출처 및 근거

ORD 기록
ord-96c71ebfff6c4ee8bb6a5aa2960c2ba3
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07915424B2

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