±-3-(1H-imidazol-1-yl)-1-(2'-(4-bromobenzyloxy)-phenyl)-1-propanol

Base Information

• Chemical Name: ±-3-(1H-imidazol-1-yl)-1-(2'-(4-bromobenzyloxy)-phenyl)-1-propanol
• CAS No.: 1440859-51-7
• Molecular Formula: C₁₉H₁₉BrN₂O₂
• Molecular Weight: 387.276
• Mol file: 1440859-51-7.mol

Synonyms:±-3-(1H-imidazol-1-yl)-1-(2'-(4-bromobenzyloxy)-phenyl)-1-propanol

Chemical Property of ±-3-(1H-imidazol-1-yl)-1-(2'-(4-bromobenzyloxy)-phenyl)-1-propanol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of ±-3-(1H-imidazol-1-yl)-1-(2'-(4-bromobenzyloxy)-phenyl)-1-propanol

There total 5 articles about ±-3-(1H-imidazol-1-yl)-1-(2'-(4-bromobenzyloxy)-phenyl)-1-propanol 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: 75.0%

1-(2-(4-bromobenzyloxy)phenyl)-3-(1H-imidazol-1-yl)-1-propanone hydrochloride (1440858-87-6) → ±-3-(1H-imidazol-1-yl)-1-(2'-(4-bromobenzyloxy)-phenyl)-1-propanol (1440859-51-7)

Guidance literature:

With sodium tetrahydroborate; In methanol; at 20 ℃;

DOI:10.1002/ardp.201200287

Reference yield:

1-(2-(4-bromobenzyloxy)phenyl)ethanone (845866-47-9) → ±-3-(1H-imidazol-1-yl)-1-(2'-(4-bromobenzyloxy)-phenyl)-1-propanol (1440859-51-7)

Guidance literature:

Multi-step reaction with 3 steps

1.1: hydrogenchloride / isopropyl alcohol; water / Reflux

2.1: water / 1 h / Reflux

2.2: 20 °C

3.1: sodium tetrahydroborate / methanol / 20 °C

With hydrogenchloride; sodium tetrahydroborate; In methanol; water; isopropyl alcohol; 1.1: |Mannich Aminomethylation;

DOI:10.1002/ardp.201200287

Reference yield:

o-hydroxyacetophenone (118-93-4,104809-67-8) → ±-3-(1H-imidazol-1-yl)-1-(2'-(4-bromobenzyloxy)-phenyl)-1-propanol (1440859-51-7)

Guidance literature:

Multi-step reaction with 4 steps

1.1: sodium ethanolate / ethanol / 0.08 h / 20 °C

1.2: 5 h / Reflux

2.1: hydrogenchloride / isopropyl alcohol; water / Reflux

3.1: water / 1 h / Reflux

3.2: 20 °C

4.1: sodium tetrahydroborate / methanol / 20 °C

With hydrogenchloride; sodium tetrahydroborate; sodium ethanolate; In methanol; ethanol; water; isopropyl alcohol; 2.1: |Mannich Aminomethylation;

DOI:10.1002/ardp.201200287

upstream raw materials:

1-(2-(4-bromobenzyloxy)phenyl)-3-(1H-imidazol-1-yl)-1-propanone hydrochloride

1-(2-(4-bromobenzyloxy)phenyl)ethanone

o-hydroxyacetophenone

1-bromomethyl-4-bromobenzene