4-Benzyloxy-5-[1-(5-tridecyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-1,5-dihydro-pyrrol-2-one

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Chemical Name:4-Benzyloxy-5-[1-(5-tridecyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-1,5-dihydro-pyrrol-2-one
CAS No.:1025931-58-1
Molecular Formula:C₂₉H₄₀N₂O₂
Molecular Weight:448.649
Hs Code.:

Synonyms:4-Benzyloxy-5-[1-(5-tridecyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-1,5-dihydro-pyrrol-2-one

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Chemical Property of 4-Benzyloxy-5-[1-(5-tridecyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-1,5-dihydro-pyrrol-2-one

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Technology Process of 4-Benzyloxy-5-[1-(5-tridecyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-1,5-dihydro-pyrrol-2-one

There total 1 articles about 4-Benzyloxy-5-[1-(5-tridecyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-1,5-dihydro-pyrrol-2-one 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:

: 113896-95-0
4-benzyloxy-1,5-dihydropyrrol-2-one

: 5-tridecyl-1H-pyrrole-2-carbaldehyde

: 1025931-58-1
4-Benzyloxy-5-[1-(5-tridecyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-1,5-dihydro-pyrrol-2-one

Guidance literature:: With sodium hydroxide; In dimethyl sulfoxide; at 60 ℃; for 8h;
DOI:10.1021/jm001003p

Reference yield:

: 1025931-58-1
4-Benzyloxy-5-[1-(5-tridecyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-1,5-dihydro-pyrrol-2-one

: 4-benzyloxy-5-[(5-tridecyl-2H-pyrrol-2-ylidene)methyl]-2,2'-bi-1H-pyrrole hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1.1: CH₂Cl₂ / 0.5 h / 0 - 5 °C

2.1: K₂CO₃; tetrakis(triphenylphosphine)palladium⁽⁰⁾ / dioxane / 90 °C

2.2: HCl / diisopropyl ether / 20 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; In 1,4-dioxane; dichloromethane; 1.1: Condensation / 2.1: Substitution / 2.2: acidolysis;
DOI:10.1021/jm001003p