2-benzyl-1-(4-(trifluoromethyl)phenyl)-1,2-dihydroisoquinolin-3(4H)-one

Base Information

Chemical Name:2-benzyl-1-(4-(trifluoromethyl)phenyl)-1,2-dihydroisoquinolin-3(4H)-one
CAS No.:1159998-10-3
Molecular Formula:C₂₃H₁₈F₃NO
Molecular Weight:381.397
Hs Code.:

Synonyms:2-benzyl-1-(4-(trifluoromethyl)phenyl)-1,2-dihydroisoquinolin-3(4H)-one

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Chemical Property of 2-benzyl-1-(4-(trifluoromethyl)phenyl)-1,2-dihydroisoquinolin-3(4H)-one

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Technology Process of 2-benzyl-1-(4-(trifluoromethyl)phenyl)-1,2-dihydroisoquinolin-3(4H)-one

There total 3 articles about 2-benzyl-1-(4-(trifluoromethyl)phenyl)-1,2-dihydroisoquinolin-3(4H)-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:

: 79128-82-8
N-(4-(trifluoromethyl)benzylidene)phenylmethanamine

: 103-80-0
phenylacetyl chloride

: 1159998-10-3
2-benzyl-1-(4-(trifluoromethyl)phenyl)-1,2-dihydroisoquinolin-3(4H)-one

Guidance literature:: N-(4-(trifluoromethyl)benzylidene)phenylmethanamine; phenylacetyl chloride; In dichloromethane; for 2h;

With trifluorormethanesulfonic acid; for 1.5h;

Reference yield:

: 100-46-9
benzylamine

: 1159998-10-3
2-benzyl-1-(4-(trifluoromethyl)phenyl)-1,2-dihydroisoquinolin-3(4H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 72 h / 20 °C / Molecular sieve; Inert atmosphere

2: toluene-4-sulfonic acid / 3.5 h / 20 °C

With toluene-4-sulfonic acid; In dichloromethane;
DOI:10.1021/jm401955h

Reference yield:

: 455-19-6
4-Trifluoromethylbenzaldehyde

: 1159998-10-3
2-benzyl-1-(4-(trifluoromethyl)phenyl)-1,2-dihydroisoquinolin-3(4H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 72 h / 20 °C / Molecular sieve; Inert atmosphere

2: toluene-4-sulfonic acid / 3.5 h / 20 °C

With toluene-4-sulfonic acid; In dichloromethane;
DOI:10.1021/jm401955h