(E)-2-fluoro-N,N-dimethyl-5-((1-oxo-1,3-dihydroisobenzofuran-4-ylimino)methyl)benzamide

Base Information

Chemical Name:(E)-2-fluoro-N,N-dimethyl-5-((1-oxo-1,3-dihydroisobenzofuran-4-ylimino)methyl)benzamide
CAS No.:1207454-82-7
Molecular Formula:C₁₈H₁₅FN₂O₃
Molecular Weight:326.327
Hs Code.:

Synonyms:(E)-2-fluoro-N,N-dimethyl-5-((1-oxo-1,3-dihydroisobenzofuran-4-ylimino)methyl)benzamide

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Chemical Property of (E)-2-fluoro-N,N-dimethyl-5-((1-oxo-1,3-dihydroisobenzofuran-4-ylimino)methyl)benzamide

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Technology Process of (E)-2-fluoro-N,N-dimethyl-5-((1-oxo-1,3-dihydroisobenzofuran-4-ylimino)methyl)benzamide

There total 6 articles about (E)-2-fluoro-N,N-dimethyl-5-((1-oxo-1,3-dihydroisobenzofuran-4-ylimino)methyl)benzamide 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: 37.0%

: 59434-19-4
4-Amino-1(3H)-isobenzofuranon

: 1207454-81-6
2-fluoro-5-formyl-N,N-dimethylbenzamide

: 1207454-82-7
(E)-2-fluoro-N,N-dimethyl-5-((1-oxo-1,3-dihydroisobenzofuran-4-ylimino)methyl)benzamide

Guidance literature:: With magnesium sulfate; In acetonitrile; for 48h; Reflux;

Reference yield:

: 641-70-3
3-nitrophthalic acid anhydride

: 1207454-82-7
(E)-2-fluoro-N,N-dimethyl-5-((1-oxo-1,3-dihydroisobenzofuran-4-ylimino)methyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium tetrahydroborate / tetrahydrofuran / 3 h / 0 °C

1.2: pH 1

2.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 3 h / 25 °C / 760.05 Torr

3.1: magnesium sulfate / acetonitrile / 48 h / Reflux

With sodium tetrahydroborate; hydrogen; magnesium sulfate; palladium 10% on activated carbon; In tetrahydrofuran; ethyl acetate; acetonitrile;

Reference yield:

: 65399-18-0
4-nitrophthalide

: 1207454-82-7
(E)-2-fluoro-N,N-dimethyl-5-((1-oxo-1,3-dihydroisobenzofuran-4-ylimino)methyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 3 h / 25 °C / 760.05 Torr

2: magnesium sulfate / acetonitrile / 48 h / Reflux

With hydrogen; magnesium sulfate; palladium 10% on activated carbon; In ethyl acetate; acetonitrile;