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2'-chloro-5'-methylfluorescein di-t-butyldimethylsilylether

Base Information
  • Chemical Name:2'-chloro-5'-methylfluorescein di-t-butyldimethylsilylether
  • CAS No.:389625-49-4
  • Molecular Formula:C33H41ClO5Si2
  • Molecular Weight:609.31
  • Hs Code.:
2'-chloro-5'-methylfluorescein di-t-butyldimethylsilylether

Synonyms:2'-chloro-5'-methylfluorescein di-t-butyldimethylsilylether

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Chemical Property of 2'-chloro-5'-methylfluorescein di-t-butyldimethylsilylether
Chemical Property:
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Technology Process of 2'-chloro-5'-methylfluorescein di-t-butyldimethylsilylether

There total 1 articles about 2'-chloro-5'-methylfluorescein di-t-butyldimethylsilylether which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 3 steps
1.1: AlCl3 / nitrobenzene / 0 - 120 °C
1.2: 48.9 percent / 0.1 M HCl / hexane
2.1: ZnCl2 / 1.08 h / 150 - 250 °C
2.2: 90 percent / 3 M HCl / 0.5 h / Heating
3.1: 37 percent Spectr. / imidazole / dimethylformamide / 12 h / 20 °C
With 1H-imidazole; aluminium trichloride; zinc(II) chloride; In nitrobenzene; N,N-dimethyl-formamide;
DOI:10.1021/ja0287377
Guidance literature:
Multi-step reaction with 3 steps
1.1: 73.3 percent / 1,3-dibromo-5,5-dimethylhydantoin; 1,1'-azobis(cyclohexanecarbonitrile); AcOH / chlorobenzene / 60 h / 40 °C
2.1: AgNO3; pyridine / acetonitrile / 15 h
2.2: acetonitrile / 12 h / 20 °C
3.1: 30 percent / AcOH; TBAF / tetrahydrofuran / 36 h / 20 °C
With pyridine; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; tetrabutyl ammonium fluoride; silver nitrate; acetic acid; 1,1'-azobis(1-cyanocyclohexanenitrile); In tetrahydrofuran; chlorobenzene; acetonitrile;
DOI:10.1021/ja0287377
Guidance literature:
Multi-step reaction with 2 steps
1.1: 73.3 percent / 1,3-dibromo-5,5-dimethylhydantoin; 1,1'-azobis(cyclohexanecarbonitrile); AcOH / chlorobenzene / 60 h / 40 °C
2.1: AgNO3; pyridine / acetonitrile / 15 h
2.2: acetonitrile / 12 h / 20 °C
With pyridine; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; silver nitrate; acetic acid; 1,1'-azobis(1-cyanocyclohexanenitrile); In chlorobenzene; acetonitrile;
DOI:10.1021/ja0287377
upstream raw materials:

phthalic anhydride

Downstream raw materials:

C52H59ClN4O5Si2

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