(E)-2-[2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)allyl]isoindole-1,3-dione

Base Information

• Chemical Name: (E)-2-[2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)allyl]isoindole-1,3-dione
• CAS No.: 858645-77-9
• Molecular Formula: C₂₇H₂₅NO₆
• Molecular Weight: 459.499
• Mol file: 858645-77-9.mol

Synonyms:(E)-2-[2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)allyl]isoindole-1,3-dione

Chemical Property of (E)-2-[2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)allyl]isoindole-1,3-dione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (E)-2-[2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)allyl]isoindole-1,3-dione

There total 5 articles about (E)-2-[2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)allyl]isoindole-1,3-dione 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: 30.0%

(E)-2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)prop-2-en-1-ol (858645-76-8) + phthalimide (136918-14-4,85-41-6) → (E)-2-[2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)allyl]isoindole-1,3-dione (858645-77-9)

Guidance literature:

With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20 ℃; for 0.75h;

DOI:10.1016/j.ejmech.2004.12.008

Reference yield:

(E)-2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)acrylic acid methyl ester (858645-75-7) → (E)-2-[2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)allyl]isoindole-1,3-dione (858645-77-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 96 percent / LiAlH₄ / tetrahydrofuran / -20 - 20 °C

2: 30 percent / diisopropyl azodicarboxylate; PPh₃ / tetrahydrofuran / 0.75 h / 20 °C

With lithium aluminium tetrahydride; di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran;

DOI:10.1016/j.ejmech.2004.12.008

Reference yield:

4-Methoxyphenylacetic acid (104-01-8) → (E)-2-[2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)allyl]isoindole-1,3-dione (858645-77-9)

Guidance literature:

Multi-step reaction with 4 steps

1: 97 percent / Et₃N; Ac₂O / 3 h / Heating

2: 64 percent / H₂SO₄ / 0.75 h / Heating

3: 96 percent / LiAlH₄ / tetrahydrofuran / -20 - 20 °C

4: 30 percent / diisopropyl azodicarboxylate; PPh₃ / tetrahydrofuran / 0.75 h / 20 °C

With lithium aluminium tetrahydride; di-isopropyl azodicarboxylate; sulfuric acid; acetic anhydride; triethylamine; triphenylphosphine; In tetrahydrofuran;

DOI:10.1016/j.ejmech.2004.12.008

upstream raw materials:

(E)-2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)prop-2-en-1-ol

phthalimide

(E)-2-(4'-methoxyphenyl)-3-(3'',4'',5'''-trimethoxyphenyl)acrylic acid methyl ester

4-Methoxyphenylacetic acid