2-Cyclohexylidene-3-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid 4-methyl ester

Base Information

Chemical Name:2-Cyclohexylidene-3-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid 4-methyl ester
CAS No.:79219-64-0
Molecular Formula:C₁₉H₂₂O₅
Molecular Weight:330.381
Hs Code.:

Synonyms:2-Cyclohexylidene-3-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid 4-methyl ester

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Chemical Property of 2-Cyclohexylidene-3-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid 4-methyl ester

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Technology Process of 2-Cyclohexylidene-3-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid 4-methyl ester

There total 3 articles about 2-Cyclohexylidene-3-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid 4-methyl ester 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: 91.0%

: 40745-21-9
dimethyl 2-cyclohexylidenesuccinate

: 123-11-5
4-methoxy-benzaldehyde

: 79219-64-0
2-Cyclohexylidene-3-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid 4-methyl ester

Guidance literature:: With potassium tert-butylate; In tert-butyl alcohol; for 1h; Ambient temperature;

Reference yield:

: 21985-20-6
3-cyclohexylidene-4-methoxy-4-oxobutanoic acid

: 79219-64-0
2-Cyclohexylidene-3-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid 4-methyl ester

Guidance literature:: Multi-step reaction with 2 steps

2: 91 percent / potassium tert.-butoxide / 2-methyl-propan-2-ol / 1 h / Ambient temperature

With potassium tert-butylate; In tert-butyl alcohol;

Reference yield:

: 108-94-1,11119-77-0,9003-41-2,9075-99-4
cyclohexanone

: 79219-64-0
2-Cyclohexylidene-3-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid 4-methyl ester

Guidance literature:: Multi-step reaction with 3 steps

3: 91 percent / potassium tert.-butoxide / 2-methyl-propan-2-ol / 1 h / Ambient temperature

With potassium tert-butylate; In tert-butyl alcohol;