Production Method 1

1746-23-2

2227355-48-6

Reaction Conditions

1.1R:C:2485728-46-7, S:BuOH, 4 h, 80°C

Reference

''Bulky-Yet-Flexible'' α-Diimine Palladium-Catalyzed Reductive Heck Cross-Coupling: Highly Anti-Markovnikov-Selective Hydroarylation of Alkene in Air

By Yang, Xu-Wen et al, Journal of Organic Chemistry, 2020, 85(18), 11750-11765

Production Method 2

1746-23-2

2227355-48-6

Reaction Conditions

1.1R:KOH, C:2106811-81-6, S:Me2CHOH, 12 h, 75°C; 75°C → rt
1.2R:mCPBA, S:CH2Cl2, 0-10°C

Reference

Pd-Catalyzed reductive Heck reaction of olefins with aryl bromides for Csp2-Csp3 bond formation

By Jin, Liqun et al, Chemical Communications (Cambridge, 2018, 54(45), 5752-5755

Production Method 3

623-26-7

35779-04-5

2227355-48-6

2919755-76-1

98-06-6

Reaction Conditions

1.1R:TMBAC, S:MeCN, 3 h, rt

Reference

Electroreduction Enables Regioselective 1,2-Diarylation of Alkenes with Two Electrophiles

By Yu, Weijie et al, Angewandte Chemie, 2023, 62(17), e202219166

Benzene, 1-(1,1-dimethylethyl)-4-[2-(4-methylphenyl)ethyl]- Raw materials

• 1,4-Dicyanobenzene
• 1-tert-Butyl-4-iodobenzene
• 4-tert-Butylstyrene

Benzene, 1-(1,1-dimethylethyl)-4-[2-(4-methylphenyl)ethyl]- Preparation Products

• Benzonitrile, 4-[2-[4-(1,1-dimethylethyl)phenyl]-1-(4-methylphenyl)ethyl]- (2919755-76-1)
• Benzene, 1-(1,1-dimethylethyl)-4-[2-(4-methylphenyl)ethyl]- (2227355-48-6)
• tert-Butylbenzene (98-06-6)

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