(E)-Ethyl 2-(6-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-en-1-yl)-1-oxophthalazin-2(1H)-yl)acetate

Base Information

Chemical Name:(E)-Ethyl 2-(6-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-en-1-yl)-1-oxophthalazin-2(1H)-yl)acetate
CAS No.:1416980-16-9
Molecular Formula:C₂₂H₁₆Cl₂F₄N₂O₃
Molecular Weight:503.28
Hs Code.:

Synonyms:(E)-Ethyl 2-(6-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-en-1-yl)-1-oxophthalazin-2(1H)-yl)acetate

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Chemical Property of (E)-Ethyl 2-(6-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-en-1-yl)-1-oxophthalazin-2(1H)-yl)acetate

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Technology Process of (E)-Ethyl 2-(6-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-en-1-yl)-1-oxophthalazin-2(1H)-yl)acetate

There total 6 articles about (E)-Ethyl 2-(6-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-en-1-yl)-1-oxophthalazin-2(1H)-yl)acetate 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: 29.0%

: 1416979-51-5
5-(1-bromo-2,2,2-trifluoroethyl)-1,3-dichloro-2-fluorobenzene

: 1416980-13-6
ethyl-2-(1-oxo-6-vinylphthalazine-2(1H)-yl) acetate

: 1416980-16-9
(E)-Ethyl 2-(6-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-en-1-yl)-1-oxophthalazin-2(1H)-yl)acetate

Guidance literature:: [2,2]bipyridinyl; copper(l) chloride; In 1,2-dichloro-benzene; at 180 ℃; for 12h; Inert atmosphere;

Reference yield:

: 6941-75-9
5-Bromoisoindoline-1,3-dione

: 1416980-16-9
(E)-Ethyl 2-(6-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-en-1-yl)-1-oxophthalazin-2(1H)-yl)acetate

Guidance literature:: Multi-step reaction with 5 steps

1: zinc; sodium hydroxide; copper(ll) sulfate pentahydrate / water / 3.5 h / 0 - 20 °C

2: hydrazine hydrate / water / 5 h / 95 °C

3: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / dimethyl sulfoxide / 2 h / 80 °C / Inert atmosphere

4: caesium carbonate / N,N-dimethyl-formamide / 8 h / 20 °C

5: [2,2]bipyridinyl; copper(l) chloride / 1,2-dichloro-benzene / 12 h / 180 °C / Inert atmosphere

With copper(ll) sulfate pentahydrate; potassium carbonate; caesium carbonate; hydrazine hydrate; sodium hydroxide; zinc; [2,2]bipyridinyl; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; copper(l) chloride; In water; dimethyl sulfoxide; N,N-dimethyl-formamide; 1,2-dichloro-benzene;

Reference yield:

: 573675-39-5
5-bromo-3-hydroxyisoindoline-1-one

: 1416980-16-9
(E)-Ethyl 2-(6-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-en-1-yl)-1-oxophthalazin-2(1H)-yl)acetate

Guidance literature:: Multi-step reaction with 4 steps

1: hydrazine hydrate / water / 5 h / 95 °C

2: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / dimethyl sulfoxide / 2 h / 80 °C / Inert atmosphere

3: caesium carbonate / N,N-dimethyl-formamide / 8 h / 20 °C

4: [2,2]bipyridinyl; copper(l) chloride / 1,2-dichloro-benzene / 12 h / 180 °C / Inert atmosphere

With potassium carbonate; caesium carbonate; hydrazine hydrate; [2,2]bipyridinyl; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; copper(l) chloride; In water; dimethyl sulfoxide; N,N-dimethyl-formamide; 1,2-dichloro-benzene;