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Tributyltin azide → HCID 178498353, 화합물

HRID 271323
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인쇄 미리보기

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HRID 271323 반응식
[CH3:1][O:2][C:3](=[O:14])[C:4]1[C:9]([Cl:10])=[CH:8][C:7]([C:11]#[N:12])=[CH:6][C:5]=1[Cl:13].[N:15]([Sn](CCCC)(CCCC)CCCC)=[N+:16]=[N-:17]>C1(C)C=CC=CC=1>[CH3:1][O:2][C:3](=[O:14])[C:4]1[C:5]([Cl:13])=[CH:6][C:7]([C:11]2[NH:17][N:16]=[N:15][N:12]=2)=[CH:8][C:9]=1[Cl:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4984872Tributyltin azideHCID 53401291Methyl 2,6-dichloro-4-cyanobenzoate

생성물 1

HCID 178498353HCID 178498353, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
100 °C

실험 절차

The mixture of 185 mg of 2,6-dichloro-4-cyanobenzoic acid methylester, 266 mg of azidotributyltin and 5 ml of toluene was stirred at 100° C. for 3 days. The reaction mixture was concentrated and diluted with ethyl acetate. After Celite filtration, the filtrate was concentrated and the residue was purified by reverse phase HPLC to obtain the title compound.

후처리

  1. concentrationThe reaction mixture was concentrated
  2. additiondiluted with ethyl acetate
  3. filtrationAfter Celite filtration
  4. concentrationthe filtrate was concentrated
  5. customthe residue was purified by reverse phase HPLC

출처 및 근거

ORD 기록
ord-2fdbb417753a459193cf47bd0c0624b8
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07452905B2

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