5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-2-(4-nitrophenyimino)thiazolidin-4-one

Base Information

Chemical Name:5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-2-(4-nitrophenyimino)thiazolidin-4-one
CAS No.:1186634-18-3
Molecular Formula:C₃₀H₂₉N₃O₄S
Molecular Weight:527.644
Hs Code.:

Synonyms:5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-2-(4-nitrophenyimino)thiazolidin-4-one

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Chemical Property of 5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-2-(4-nitrophenyimino)thiazolidin-4-one

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Technology Process of 5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-2-(4-nitrophenyimino)thiazolidin-4-one

There total 5 articles about 5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-2-(4-nitrophenyimino)thiazolidin-4-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: 95.0%

: 63500-84-5
3-methyl-2-(4-nitro-phenylimino)-thiazolidin-4-one

: 1186634-26-3
4-(4-cyclohexylbenzyloxy)benzaldehyde

: 1186634-18-3
5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-2-(4-nitrophenyimino)thiazolidin-4-one

Guidance literature:: With piperidine; In ethanol; for 14h; Reflux;

Reference yield:

: 20029-52-1
4-cyclohexylbenzoic acid

: 1186634-18-3
5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-2-(4-nitrophenyimino)thiazolidin-4-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: sulfuric acid / 5 h / Reflux

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C

2.2: 0 °C

3.1: thionyl chloride / dichloromethane / 0.5 h / 0 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 20 - 60 °C

5.1: piperidine / ethanol / 14 h / Reflux

With piperidine; lithium aluminium tetrahydride; thionyl chloride; sulfuric acid; potassium carbonate; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 208259-47-6
4-cyclohexylphenylmethyl alcohol

: 1186634-18-3
5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-2-(4-nitrophenyimino)thiazolidin-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / dichloromethane / 0.5 h / 0 °C

2: potassium carbonate / N,N-dimethyl-formamide / 20 - 60 °C

3: piperidine / ethanol / 14 h / Reflux

With piperidine; thionyl chloride; potassium carbonate; In ethanol; dichloromethane; N,N-dimethyl-formamide;