1,2-bis{6-[4-(4-(4-hexyloxyphenyl)-2,3-difluorophenyl)phenyloxy]hexyloxy}benzene

Base Information

• Chemical Name: 1,2-bis{6-[4-(4-(4-hexyloxyphenyl)-2,3-difluorophenyl)phenyloxy]hexyloxy}benzene
• CAS No.: 1608153-12-3
• Molecular Formula: C₆₆H₇₄F₄O₆
• Molecular Weight: 1039.3

Synonyms:1,2-bis{6-[4-(4-(4-hexyloxyphenyl)-2,3-difluorophenyl)phenyloxy]hexyloxy}benzene

Chemical Property of 1,2-bis{6-[4-(4-(4-hexyloxyphenyl)-2,3-difluorophenyl)phenyloxy]hexyloxy}benzene

Chemical Property:

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Technology Process of 1,2-bis{6-[4-(4-(4-hexyloxyphenyl)-2,3-difluorophenyl)phenyloxy]hexyloxy}benzene

There total 4 articles about 1,2-bis{6-[4-(4-(4-hexyloxyphenyl)-2,3-difluorophenyl)phenyloxy]hexyloxy}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: 20.0%

1,2-bis(bromohexyloxy)benzene + 4-(4-hexyloxyphenyl)-1-(4-hydroxyphenyl)-2,3-difluorobenzene (1608153-10-1) → 1,2-bis{6-[4-(4-(4-hexyloxyphenyl)-2,3-difluorophenyl)phenyloxy]hexyloxy}benzene (1608153-12-3)

Guidance literature:

With potassium carbonate; In cyclohexanone; at 120 ℃; for 10h;

DOI:10.1039/c4tc00001c

Reference yield:

1-bromo-hexane (111-25-1) → 1,2-bis{6-[4-(4-(4-hexyloxyphenyl)-2,3-difluorophenyl)phenyloxy]hexyloxy}benzene (1608153-12-3)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium carbonate / cyclohexanone / 9 h / 110 °C

2: hydrogenchloride / ethanol; water / 2 h / 25 °C

3: potassium carbonate / cyclohexanone / 10 h / 120 °C

With hydrogenchloride; potassium carbonate; In ethanol; water; cyclohexanone;

DOI:10.1039/c4tc00001c

Reference yield:

4-hydroxylphenyl-1-[4-(2-tetrahydropyranyloxy)phenyl]-2,3-difluorobenzene (1608153-06-5) → 1,2-bis{6-[4-(4-(4-hexyloxyphenyl)-2,3-difluorophenyl)phenyloxy]hexyloxy}benzene (1608153-12-3)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium carbonate / cyclohexanone / 9 h / 110 °C

2: hydrogenchloride / ethanol; water / 2 h / 25 °C

3: potassium carbonate / cyclohexanone / 10 h / 120 °C

With hydrogenchloride; potassium carbonate; In ethanol; water; cyclohexanone;

DOI:10.1039/c4tc00001c

upstream raw materials:

1-bromo-hexane

4-(4-hexyloxyphenyl)-1-(4-hydroxyphenyl)-2,3-difluorobenzene

4-hydroxylphenyl-1-[4-(2-tetrahydropyranyloxy)phenyl]-2,3-difluorobenzene

4-hexyloxylphenyl-1-[4-(2-tetrahydropyranyloxy)phenyl]-2,3-difluorobenzene

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