trans-1,4-dimethoxy-2,3,5-trimethyl-6-(3',7'-dimethyl-8'-bromo-2',6'-octadienyl)benzene

Base Information

Chemical Name:trans-1,4-dimethoxy-2,3,5-trimethyl-6-(3',7'-dimethyl-8'-bromo-2',6'-octadienyl)benzene
CAS No.:66958-63-2
Molecular Formula:C₂₁H₃₁BrO₂
Molecular Weight:395.38
Hs Code.:

Synonyms:trans-1,4-dimethoxy-2,3,5-trimethyl-6-(3',7'-dimethyl-8'-bromo-2',6'-octadienyl)benzene

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Chemical Property of trans-1,4-dimethoxy-2,3,5-trimethyl-6-(3',7'-dimethyl-8'-bromo-2',6'-octadienyl)benzene

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Technology Process of trans-1,4-dimethoxy-2,3,5-trimethyl-6-(3',7'-dimethyl-8'-bromo-2',6'-octadienyl)benzene

There total 3 articles about trans-1,4-dimethoxy-2,3,5-trimethyl-6-(3',7'-dimethyl-8'-bromo-2',6'-octadienyl)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: 87.6%

: 28'-chloroubiquinol-7 dibenzyl ether

: 66958-61-0
trans-1,4-dimethoxy-2,3,5-trimethyl-6-(3',7'-dimethyl-6'-hydroxy-2',7'-octadienyl)benzene

: 66958-63-2
trans-1,4-dimethoxy-2,3,5-trimethyl-6-(3',7'-dimethyl-8'-bromo-2',6'-octadienyl)benzene

Guidance literature:: With dibromo sulfoxide;

Reference yield:

: 66958-61-0
trans-1,4-dimethoxy-2,3,5-trimethyl-6-(3',7'-dimethyl-6'-hydroxy-2',7'-octadienyl)benzene

: 66958-63-2
trans-1,4-dimethoxy-2,3,5-trimethyl-6-(3',7'-dimethyl-8'-bromo-2',6'-octadienyl)benzene

Guidance literature:: With dibromo sulfoxide; In tetrahydrofuran;

Reference yield:

: 66958-60-9
3-[(E)-5-(2,5-Dimethoxy-3,4,6-trimethyl-phenyl)-3-methyl-pent-3-enyl]-2,2-dimethyl-oxirane

: 66958-63-2
trans-1,4-dimethoxy-2,3,5-trimethyl-6-(3',7'-dimethyl-8'-bromo-2',6'-octadienyl)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: lithium diisopropyl amide / tetrahydrofuran

2: dibromo sulfoxide / tetrahydrofuran

With dibromo sulfoxide; lithium diisopropyl amide; In tetrahydrofuran;