(2-(Benzyloxy)-5-bromophenyl)methanol

Base Information

• Chemical Name: (2-(Benzyloxy)-5-bromophenyl)methanol
• CAS No.: 177759-46-5
• Molecular Formula: C14H13BrO2
• Molecular Weight: 293.16
• Hs Code.: 2909499000
• DSSTox Substance ID: DTXSID60358458
• Nikkaji Number: J2.381.791H
• Wikidata: Q82139041
• Mol file: 177759-46-5.mol

Synonyms:(2-(Benzyloxy)-5-bromophenyl)methanol;177759-46-5;2-Benzylox-5-bromobenzyl alcohol;(5-bromo-2-phenylmethoxyphenyl)methanol;[2-(benzyloxy)-5-bromophenyl]methanol;2-Benzyloxy-5-bromo-benzyl alcohol;SCHEMBL4680227;2-benzyloxy-5-bromobenzylalcohol;DTXSID60358458;2-benzyloxy-5-bromobenzyl alcohol;CHA75946;2-(Benzyloxy)-5-bromobenzyl alcohol;MFCD03716182;AKOS003748742;(2-benzyloxy-5-bromo-phenyl)-methanol;5-Bromo-2-(phenylmethoxy)benzenemethanol;BS-21834;CS-0210251;FT-0704170;{5-bromo-2-[(phenylmethyl)oxy]phenyl}methanol;F79955;SR-01000255879;SR-01000255879-1;Z26223710

Chemical Property of (2-(Benzyloxy)-5-bromophenyl)methanol

Chemical Property:

• PSA: 29.46000
• LogP: 3.52040
• XLogP3: 3.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 292.00989
• Heavy Atom Count: 17
• Complexity: 216

Purity/Quality:

99% ^*data from raw suppliers

2-Benzylox-5-bromobenzylalcohol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)COC2=C(C=C(C=C2)Br)CO

Technology Process of (2-(Benzyloxy)-5-bromophenyl)methanol

There total 5 articles about (2-(Benzyloxy)-5-bromophenyl)methanol 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: 100.0%

2-benzyloxy-5-bromobenzaldehyde (121124-94-5) → [2-(Benzyloxy)-5-bromophenyl]methanol (177759-46-5)

Guidance literature:

With methanol; sodium tetrahydroborate; at 20 ℃;

Reference yield: 94.0%

benzyl bromide (100-39-0) + 5-bromo-2-hydroxybenzyl alcohol (2316-64-5) → [2-(Benzyloxy)-5-bromophenyl]methanol (177759-46-5)

Guidance literature:

5-bromo-2-hydroxybenzyl alcohol; With sodium hydroxide; In ethanol; water; for 0.166667h;

benzyl bromide; In ethanol; water; at 20 ℃;

Reference yield:

5-bromosalicyclaldehyde (1761-61-1) → [2-(Benzyloxy)-5-bromophenyl]methanol (177759-46-5)

Guidance literature:

Multi-step reaction with 2 steps

1: K₂CO₃ / acetone / 60 °C

2: NaBH₄ / tetrahydrofuran; methanol / 0 - 20 °C

With sodium tetrahydroborate; potassium carbonate; In tetrahydrofuran; methanol; acetone;

DOI:10.1016/j.tetlet.2006.09.059

upstream raw materials:

benzyl bromide

5-bromo-2-hydroxybenzyl alcohol

2-benzyloxy-5-bromobenzaldehyde

5-bromosalicyclaldehyde

Downstream raw materials:

[2-(2-benzyloxy-5-bromo-benzyloxymethoxy)-ethyl]-trimethyl-silane