2-(2-Benzenesulfinyl-ethyl)-2-(benzhydrylidene-amino)-5-oxo-hexanenitrile

Base Information

Chemical Name:2-(2-Benzenesulfinyl-ethyl)-2-(benzhydrylidene-amino)-5-oxo-hexanenitrile
CAS No.:137283-36-4
Molecular Formula:C₂₇H₂₆N₂O₂S
Molecular Weight:442.582
Hs Code.:

Synonyms:2-(2-Benzenesulfinyl-ethyl)-2-(benzhydrylidene-amino)-5-oxo-hexanenitrile

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Chemical Property of 2-(2-Benzenesulfinyl-ethyl)-2-(benzhydrylidene-amino)-5-oxo-hexanenitrile

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Technology Process of 2-(2-Benzenesulfinyl-ethyl)-2-(benzhydrylidene-amino)-5-oxo-hexanenitrile

There total 3 articles about 2-(2-Benzenesulfinyl-ethyl)-2-(benzhydrylidene-amino)-5-oxo-hexanenitrile 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: 85.0%

: 137283-21-7
4-Benzenesulfinyl-2-(benzhydrylidene-amino)-butyronitrile

: 78-94-4,25038-87-3
methyl vinyl ketone

: 137283-36-4
2-(2-Benzenesulfinyl-ethyl)-2-(benzhydrylidene-amino)-5-oxo-hexanenitrile

Guidance literature:: With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate; at 60 ℃; for 1h;
DOI:10.1080/00397919108021572

Reference yield:

: 70591-20-7
N-(diphenylmethylene)aminoacetonitrile

: 137283-36-4
2-(2-Benzenesulfinyl-ethyl)-2-(benzhydrylidene-amino)-5-oxo-hexanenitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / K₂CO₃, benzyltriethylammonium chloride (TEBACl) / 1 h / 60 °C

2: 85 percent / K₂CO₃, benzyltriethylammonium chloride (TEBACl) / 1 h / 60 °C

With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate;
DOI:10.1080/00397919108021572

Reference yield:

: 20451-53-0
Phenyl vinyl sulfoxide

: 137283-36-4
2-(2-Benzenesulfinyl-ethyl)-2-(benzhydrylidene-amino)-5-oxo-hexanenitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / K₂CO₃, benzyltriethylammonium chloride (TEBACl) / 1 h / 60 °C

2: 85 percent / K₂CO₃, benzyltriethylammonium chloride (TEBACl) / 1 h / 60 °C

With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate;
DOI:10.1080/00397919108021572