4-(4-Heptyl-cyclohexyl)-benzamide

Base Information

Chemical Name:4-(4-Heptyl-cyclohexyl)-benzamide
CAS No.:73163-48-1
Molecular Formula:C₂₀H₃₁NO
Molecular Weight:301.472
Hs Code.:

Synonyms:4-(4-Heptyl-cyclohexyl)-benzamide

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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 4-(4-Heptyl-cyclohexyl)-benzamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4-(4-Heptyl-cyclohexyl)-benzamide

There total 11 articles about 4-(4-Heptyl-cyclohexyl)-benzamide 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:

: 16618-75-0
4-n-heptylcyclohexanone

: 73163-48-1
4-(4-Heptyl-cyclohexyl)-benzamide

Guidance literature:: Multi-step reaction with 7 steps

1: 2.) 10percent aq. HCl / 1.) diethyl ether, 1 h, heating

2: p-toluenesulfonic acid / toluene / Heating

3: H₂ / 10percent Pd/C / ethanol

4: AlCl₃ / 1,2-dichloro-ethane / 0.5 h

5: aq. NaOH, Br₂ / dioxane / 3 h / 35 - 40 °C

6: SOCl₂ / 1 h / Heating

7: 25percent aq. NH₄OH

With hydrogenchloride; ammonium hydroxide; sodium hydroxide; aluminium trichloride; thionyl chloride; hydrogen; bromine; toluene-4-sulfonic acid; palladium on activated charcoal; In 1,4-dioxane; ethanol; 1,2-dichloro-ethane; toluene;

Reference yield:

: phenylmagnesium bromide

: 73163-48-1
4-(4-Heptyl-cyclohexyl)-benzamide

Guidance literature:: Multi-step reaction with 7 steps

1: 2.) 10percent aq. HCl / 1.) diethyl ether, 1 h, heating

2: p-toluenesulfonic acid / toluene / Heating

3: H₂ / 10percent Pd/C / ethanol

4: AlCl₃ / 1,2-dichloro-ethane / 0.5 h

5: aq. NaOH, Br₂ / dioxane / 3 h / 35 - 40 °C

6: SOCl₂ / 1 h / Heating

7: 25percent aq. NH₄OH

With hydrogenchloride; ammonium hydroxide; sodium hydroxide; aluminium trichloride; thionyl chloride; hydrogen; bromine; toluene-4-sulfonic acid; palladium on activated charcoal; In 1,4-dioxane; ethanol; 1,2-dichloro-ethane; toluene;

Reference yield:

: 88069-98-1
(4-n-heptylcyclohexen-1-yl)-benzene

: 73163-48-1
4-(4-Heptyl-cyclohexyl)-benzamide

Guidance literature:: Multi-step reaction with 5 steps

1: H₂ / 10percent Pd/C / ethanol

2: AlCl₃ / 1,2-dichloro-ethane / 0.5 h

3: aq. NaOH, Br₂ / dioxane / 3 h / 35 - 40 °C

4: SOCl₂ / 1 h / Heating

5: 25percent aq. NH₄OH

With ammonium hydroxide; sodium hydroxide; aluminium trichloride; thionyl chloride; hydrogen; bromine; palladium on activated charcoal; In 1,4-dioxane; ethanol; 1,2-dichloro-ethane;