2-((E)-cyclohexylidenethylidene)-cyclohexanone

Base Information

Chemical Name:2-((E)-cyclohexylidenethylidene)-cyclohexanone
CAS No.:29179-11-1
Molecular Formula:C₁₄H₂₀O
Molecular Weight:204.312
Hs Code.:

2-((<i>E</i>)-cyclohexylidenethylidene)-cyclohexanone

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-((E)-cyclohexylidenethylidene)-cyclohexanone

Chemical Property:

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Technology Process of 2-((E)-cyclohexylidenethylidene)-cyclohexanone

There total 4 articles about 2-((E)-cyclohexylidenethylidene)-cyclohexanone 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:

: 1940-19-8
1-vinylcyclohexanol

: 29179-11-1
2-((E)-cyclohexylidenethylidene)-cyclohexanone

Guidance literature:: Multi-step reaction with 3 steps

1: Erhitzen auf dem Dampfbad, Versetzen des abgekuehlten Reaktionsgemisches mit Trichloressigsaeure und Eisessig, 1 1/2-stdg. Erwaermen auf 55grad und Behandeln des Reaktionsprodukts mit 10 prozentig. methanol. KOH

2: benzene; acetic acid; CrO₃ / 0 - 70 °C

3: diluted aq. NaOH solution

With chromium(VI) oxide; sodium hydroxide; acetic acid; benzene;

Reference yield:

: 932-89-8
2-cyclohexylidene ethanol

: 29179-11-1
2-((E)-cyclohexylidenethylidene)-cyclohexanone

Guidance literature:: Multi-step reaction with 2 steps

1: benzene; acetic acid; CrO₃ / 0 - 70 °C

2: diluted aq. NaOH solution

With chromium(VI) oxide; sodium hydroxide; acetic acid; benzene;

Reference yield:

: 78-27-3
1-Ethynylcyclohexan-1-ol

: 29179-11-1
2-((E)-cyclohexylidenethylidene)-cyclohexanone

Guidance literature:: Multi-step reaction with 4 steps

1: palladium; ethanol / Hydrogenation

2: Erhitzen auf dem Dampfbad, Versetzen des abgekuehlten Reaktionsgemisches mit Trichloressigsaeure und Eisessig, 1 1/2-stdg. Erwaermen auf 55grad und Behandeln des Reaktionsprodukts mit 10 prozentig. methanol. KOH

3: benzene; acetic acid; CrO₃ / 0 - 70 °C

4: diluted aq. NaOH solution

With chromium(VI) oxide; sodium hydroxide; ethanol; palladium; acetic acid; benzene;