1-(2-phenyl-2-oxoethyl)-4-(2,2-dicyclohexyl-1-oxoethyl)benzene

Base Information

• Chemical Name: 1-(2-phenyl-2-oxoethyl)-4-(2,2-dicyclohexyl-1-oxoethyl)benzene
• CAS No.: 235103-10-3
• Molecular Formula: C₂₈H₃₄O₂
• Molecular Weight: 402.577
• Mol file: 235103-10-3.mol

Synonyms:1-(2-phenyl-2-oxoethyl)-4-(2,2-dicyclohexyl-1-oxoethyl)benzene

Chemical Property of 1-(2-phenyl-2-oxoethyl)-4-(2,2-dicyclohexyl-1-oxoethyl)benzene

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-(2-phenyl-2-oxoethyl)-4-(2,2-dicyclohexyl-1-oxoethyl)benzene

There total 5 articles about 1-(2-phenyl-2-oxoethyl)-4-(2,2-dicyclohexyl-1-oxoethyl)benzene 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: 63.0%

2,2-dicyclohexyl-1-[4-(2-phenyl-[1,3]dithian-2-ylmethyl)-phenyl]-ethanone → 1-(2-phenyl-2-oxoethyl)-4-(2,2-dicyclohexyl-1-oxoethyl)benzene (235103-10-3)

Guidance literature:

With mercury dichloride; mercury(II) oxide; In methanol; water; for 5h; Heating;

DOI:10.1021/jo990172i

Reference yield:

dicyclohexylacetic acid chloride (92373-44-9) → 1-(2-phenyl-2-oxoethyl)-4-(2,2-dicyclohexyl-1-oxoethyl)benzene (235103-10-3)

Guidance literature:

Multi-step reaction with 4 steps

1.1: AlCl₃ / 1 h

2.1: N-bromosuccinimide; benzoyl peroxide / CCl₄ / 24 h / Heating

3.1: n-BuLi / tetrahydrofuran; hexane / 1 h / -40 °C

3.2: tetrahydrofuran; hexane / 2 h / -40 °C

4.1: 63 percent / HgCl₂; HgO / methanol; H₂O / 5 h / Heating

With N-Bromosuccinimide; n-butyllithium; aluminium trichloride; mercury dichloride; mercury(II) oxide; dibenzoyl peroxide; In tetrahydrofuran; methanol; tetrachloromethane; hexane; water; 1.1: Acylation / 2.1: Bromination / 3.1: Metallation / 3.2: Substitution / 4.1: Hydrolysis;

DOI:10.1021/jo990172i

Reference yield:

dicyclohexylacetic acid (52034-92-1) → 1-(2-phenyl-2-oxoethyl)-4-(2,2-dicyclohexyl-1-oxoethyl)benzene (235103-10-3)

Guidance literature:

Multi-step reaction with 5 steps

1.1: thionyl chloride / CH₂Cl₂ / 1.5 h / Heating

2.1: AlCl₃ / 1 h

3.1: N-bromosuccinimide; benzoyl peroxide / CCl₄ / 24 h / Heating

4.1: n-BuLi / tetrahydrofuran; hexane / 1 h / -40 °C

4.2: tetrahydrofuran; hexane / 2 h / -40 °C

5.1: 63 percent / HgCl₂; HgO / methanol; H₂O / 5 h / Heating

With N-Bromosuccinimide; n-butyllithium; aluminium trichloride; thionyl chloride; mercury dichloride; mercury(II) oxide; dibenzoyl peroxide; In tetrahydrofuran; methanol; tetrachloromethane; hexane; dichloromethane; water; 1.1: Chlorination / 2.1: Acylation / 3.1: Bromination / 4.1: Metallation / 4.2: Substitution / 5.1: Hydrolysis;

DOI:10.1021/jo990172i

upstream raw materials:

dicyclohexylacetic acid chloride

dicyclohexylacetic acid

2,2-dicyclohexyl-1-(4'-methyl)phenylethanone

2,2-dicyclohexyl-1-(4'-bromomethyl)phenylethanone

Downstream raw materials:

1-(2-phenyl-2-diazoethyl)-4-(2,2-dicyclohexyl-1-oxoethyl)benzene