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Cyanuric chloride → 2-(4-Biphenylyl)-4,6-dichloro-1,3,5-triazine

HRID 1857944
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인쇄 미리보기

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HRID 1857944 반응식
[C:1]1([C:7]2[CH:12]=[CH:11][C:10]([Mg]Br)=[CH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N:15]1[C:22]([Cl:23])=[N:21][C:19](Cl)=[N:18][C:16]=1[Cl:17]>C1C=CC=CC=1>[C:7]1([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH:12]=[CH:11][C:10]([C:19]2[N:21]=[C:22]([Cl:23])[N:15]=[C:16]([Cl:17])[N:18]=2)=[CH:9][CH:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7954Cyanuric chlorideHCID 178419618HCID 178419618, 화합물

생성물 1

HCID 223522432-(4-Biphenylyl)-4,6-dichloro-1,3,5-triazine수율 43%

시약·촉매·용매 1

HCID 241Benzene용매

반응 조건

온도
0 °C

실험 절차

A mixture of 4-phenyl-phenyl magnesium bromide (prepared from 4-bromobiphenyl (7.75 g, 33 mmol) and magnesium turnings (0.83 g, 35 mmol) in 40 mL ether) and cyanuric chloride (4.00 g, 21.7 mmol) in benzene (90 mL) was stirred at 0° C. for 90 minutes. The reaction was evaporated to dryness, and the residue was flash chromatographed on silica gel with 50% hexanes/methylene chloride to provide the desired compound (2.80 g, 43%).

후처리

  1. customThe reaction was evaporated to dryness
  2. customchromatographed on silica gel with 50% hexanes/methylene chloride

출처 및 근거

ORD 기록
ord-5378414d1feb463ebda5f276a9804101
출처 데이터셋
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06150362

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