2-(3-fluoro-5-hydroxyphenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

Base Information

Chemical Name:2-(3-fluoro-5-hydroxyphenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide
CAS No.:1245607-48-0
Molecular Formula:C₁₃H₁₀FNO₃S
Molecular Weight:279.292
Hs Code.:

Synonyms:2-(3-fluoro-5-hydroxyphenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-(3-fluoro-5-hydroxyphenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

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Technology Process of 2-(3-fluoro-5-hydroxyphenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

There total 3 articles about 2-(3-fluoro-5-hydroxyphenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide 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:

Reference yield: 96.0%

: 433939-27-6
3-bromo-5-fluorophenol

: 936-16-3
2,3-dihydro-1,2-benzisothiazole 1,1-dioxide

: 1245607-48-0
2-(3-fluoro-5-hydroxyphenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

Guidance literature:: With copper(l) iodide; potassium carbonate; N,N`-dimethylethylenediamine; In acetonitrile; at 70 ℃; for 16h; Inert atmosphere;
DOI:10.1021/acs.jmedchem.6b00685

Reference yield:

: 1245607-52-6
2-(3-(benzyloxy)-5-fluorophenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

: 1245607-48-0
2-(3-fluoro-5-hydroxyphenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

Guidance literature:: With hydrogen; palladium on carbon; In methanol; at 20 ℃; for 1.5h;

Reference yield:

: 81-07-2
saccharin

: 1245607-48-0
2-(3-fluoro-5-hydroxyphenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

Guidance literature:: Multi-step reaction with 2 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 0 - 20 °C / Inert atmosphere

2: potassium carbonate; copper(l) iodide; N,N`-dimethylethylenediamine / acetonitrile / 16 h / 70 °C / Inert atmosphere

With copper(l) iodide; lithium aluminium tetrahydride; potassium carbonate; N,N`-dimethylethylenediamine; In tetrahydrofuran; acetonitrile;
DOI:10.1021/acs.jmedchem.6b00685