(E)-2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-1-methoxy-3-phenyl-prop-(Z)-ylideneamino]-3-phenyl-acrylic acid tert-butyl ester

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Chemical Name:(E)-2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-1-methoxy-3-phenyl-prop-(Z)-ylideneamino]-3-phenyl-acrylic acid tert-butyl ester
CAS No.:126181-22-4
Molecular Formula:C₃₁H₃₀N₂O₅
Molecular Weight:510.59
Hs Code.:

Synonyms:(E)-2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-1-methoxy-3-phenyl-prop-(Z)-ylideneamino]-3-phenyl-acrylic acid tert-butyl ester

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Chemical Property of (E)-2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-1-methoxy-3-phenyl-prop-(Z)-ylideneamino]-3-phenyl-acrylic acid tert-butyl ester

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Technology Process of (E)-2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-1-methoxy-3-phenyl-prop-(Z)-ylideneamino]-3-phenyl-acrylic acid tert-butyl ester

There total 2 articles about (E)-2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-1-methoxy-3-phenyl-prop-(Z)-ylideneamino]-3-phenyl-acrylic acid tert-butyl ester 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: 60.0%

: 126181-19-9
N-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-1-methoxy-3-phenyl-prop-(Z)-ylidene]-oxalamic acid tert-butyl ester

: 16721-45-2
triphenyl(phenylmethylene)phosphorane

: 126181-22-4
(E)-2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-1-methoxy-3-phenyl-prop-(Z)-ylideneamino]-3-phenyl-acrylic acid tert-butyl ester

: 791-28-6
Triphenylphosphine oxide

Guidance literature:: In toluene; for 4h; Heating;
DOI:10.1016/S0040-4039(00)99405-X

Reference yield:

: 1449-46-3
benzyltriphenylphosphonium bromide

: 126181-22-4
(E)-2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-1-methoxy-3-phenyl-prop-(Z)-ylideneamino]-3-phenyl-acrylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: t-BuOK

2: 60 percent / toluene / 4 h / Heating

With potassium tert-butylate; In toluene;
DOI:10.1016/S0040-4039(00)99405-X