1-(3-Bromo-propoxy)-3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-benzene

Base Information

• Chemical Name: 1-(3-Bromo-propoxy)-3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-benzene
• CAS No.: 176216-57-2
• Molecular Formula: C₃₅H₄₇BrO₅
• Molecular Weight: 627.659
• Mol file: 176216-57-2.mol

Synonyms:1-(3-Bromo-propoxy)-3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-benzene

Chemical Property of 1-(3-Bromo-propoxy)-3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-benzene

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-(3-Bromo-propoxy)-3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-benzene

There total 10 articles about 1-(3-Bromo-propoxy)-3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-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: 96.0%

3-{3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-phenoxy}-propan-1-ol (216968-15-9) → 1-(3-Bromo-propoxy)-3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-benzene (176216-57-2)

Guidance literature:

With carbon tetrabromide; triphenylphosphine; In tetrahydrofuran; at 20 ℃; for 12h;

DOI:10.1016/S0040-4020(98)00851-5

Reference yield: 95.0%

1,3-dibromo-propane (109-64-8) + 3,5-Bis-[3-(4-tert-butyl-phenoxy)-propoxy]-phenol (171369-23-6) → 1-(3-Bromo-propoxy)-3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-benzene (176216-57-2)

Guidance literature:

With potassium carbonate; In acetone; for 8h; Heating;

DOI:10.1016/0040-4020(96)00088-9

Reference yield:

1-bromo-3-(4'-tert-butylphenyloxy)propane (3245-63-4) → 1-(3-Bromo-propoxy)-3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-benzene (176216-57-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 91 percent / 18-crown-6; K₂CO₃ / tetrahydrofuran / 24 h / Heating

2: 96 percent / CBr₄; PPh₃ / tetrahydrofuran / 12 h / 20 °C

With 18-crown-6 ether; carbon tetrabromide; potassium carbonate; triphenylphosphine; In tetrahydrofuran; 1: Alkylation / 2: Bromination;

DOI:10.1016/S0040-4020(98)00851-5

upstream raw materials:

1,3-dibromo-propane

3,5-Bis-[3-(4-tert-butyl-phenoxy)-propoxy]-phenol

3-{3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-phenoxy}-propan-1-ol

3,5-dihydroxyphenol

Downstream raw materials:

3-[3,5-bis-(3-{3,5-bis-[3-(4-tert-butyl-phenoxy)-propoxy]-phenoxy}-propoxy)-phenoxy]-propan-1-ol

C₇₉H₁₀₃BrO₁₃