1-Benzyl-3-{2-[2-phenyl-eth-(E)-ylideneamino]-phenyl}-pyrrolidine-2,5-dione

Base Information

Chemical Name:1-Benzyl-3-{2-[2-phenyl-eth-(E)-ylideneamino]-phenyl}-pyrrolidine-2,5-dione
CAS No.:78914-32-6
Molecular Formula:C₂₅H₂₂N₂O₂
Molecular Weight:382.462
Hs Code.:

Synonyms:1-Benzyl-3-{2-[2-phenyl-eth-(E)-ylideneamino]-phenyl}-pyrrolidine-2,5-dione

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Chemical Property of 1-Benzyl-3-{2-[2-phenyl-eth-(E)-ylideneamino]-phenyl}-pyrrolidine-2,5-dione

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Technology Process of 1-Benzyl-3-{2-[2-phenyl-eth-(E)-ylideneamino]-phenyl}-pyrrolidine-2,5-dione

There total 1 articles about 1-Benzyl-3-{2-[2-phenyl-eth-(E)-ylideneamino]-phenyl}-pyrrolidine-2,5-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:

: 122-78-1
phenylacetaldehyde

: 112616-41-8
N-benzyl-3(o-amino)phenyl pyrrolidine-2,5-dione

: 78914-32-6
1-Benzyl-3-{2-[2-phenyl-eth-(E)-ylideneamino]-phenyl}-pyrrolidine-2,5-dione

Guidance literature:: DOI:10.1021/ja00405a089

Reference yield: 30.0%

: 78914-32-6
1-Benzyl-3-{2-[2-phenyl-eth-(E)-ylideneamino]-phenyl}-pyrrolidine-2,5-dione

: 78914-35-9
(2S,3'S)-2,1'-Dibenzyl-1,2-dihydro-spiro[indole-3,3'-pyrrolidine]-2',5'-dione

Guidance literature:: With sodium t-butanolate; In tert-butyl alcohol;
DOI:10.1021/ja00405a089

Reference yield:

: 78914-32-6
1-Benzyl-3-{2-[2-phenyl-eth-(E)-ylideneamino]-phenyl}-pyrrolidine-2,5-dione

: 78954-14-0
C₂₇H₂₄N₂O₂

Guidance literature:: Multi-step reaction with 3 steps

1: 30 percent / t-BuONa, t-BuOH / 2-methyl-propan-2-ol

2: 2,) NaBH₄, H+ / 1.) room temperature

3: HCOOH / 18 h / Ambient temperature

With sodium tetrahydroborate; formic acid; hydrogen cation; sodium t-butanolate; tert-butyl alcohol; In tert-butyl alcohol;
DOI:10.1021/ja00405a089