1-[2-(Benzyloxy)-5-bromophenyl]ethanone

Base Information

• Chemical Name: 1-[2-(Benzyloxy)-5-bromophenyl]ethanone
• CAS No.: 69822-20-4
• Molecular Formula: C15H13BrO2
• Molecular Weight: 305.171
• DSSTox Substance ID: DTXSID00497350
• Wikidata: Q82346800

Synonyms:1-[2-(benzyloxy)-5-bromophenyl]ethanone;69822-20-4;1-(5-Bromo-2-phenylmethoxyphenyl)ethanone;Ethanone, 1-[5-bromo-2-(phenylmethoxy)phenyl]-;1-(2-(Benzyloxy)-5-bromophenyl)ethanone;1-[2-(benzyloxy)-5-bromophenyl]ethan-1-one;SCHEMBL6452235;DTXSID00497350;KXWRALKIRNASMG-UHFFFAOYSA-N;5'-bromo-2'-benzyloxy-acetophenone;AKOS008911861;A1-05686

Chemical Property of 1-[2-(Benzyloxy)-5-bromophenyl]ethanone

Chemical Property:

• XLogP3: 3.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 304.00989
• Heavy Atom Count: 18
• Complexity: 274

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)C1=C(C=CC(=C1)Br)OCC2=CC=CC=C2

Technology Process of 1-[2-(Benzyloxy)-5-bromophenyl]ethanone

There total 1 articles about 1-[2-(Benzyloxy)-5-bromophenyl]ethanone 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: 98.0%

5-Bromo-2-hydroxyacetophenone (1450-75-5) + benzyl bromide (100-39-0) → 1-(2-(benzyloxy)-5-bromophenyl)ethanone (69822-20-4)

Guidance literature:

5-Bromo-2-hydroxyacetophenone; With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.25h; Inert atmosphere;

benzyl bromide; In N,N-dimethyl-formamide; for 3h; Inert atmosphere;

DOI:10.1016/j.carres.2014.04.005

Reference yield: 100.0%

1-(2-(benzyloxy)-5-bromophenyl)ethanone (69822-20-4) → 1-(2-(benzyloxy)-5-bromophenyl)-1-ethanol

Guidance literature:

With methanol; sodium tetrahydroborate; at 0 ℃; for 1h;

Reference yield: 96.0%

2,3-dihydro-benzo[1,4]dioxin-6-carbaldehyde (29668-44-8) + 1-(2-(benzyloxy)-5-bromophenyl)ethanone (69822-20-4) → 1-(2-benzyloxy-5-bromophenyl)-3-(6-benzodioxan-1,4-yl)propenone (96755-14-5)

Guidance literature:

With sodium hydroxide; In ethanol; for 40h; Ambient temperature;

DOI:10.1007/BF00519934

upstream raw materials:

5-Bromo-2-hydroxyacetophenone

benzyl bromide

Downstream raw materials:

(E)-1-(2-Benzyloxy-5-bromo-phenyl)-3-(3,6-dimethyl-benzofuran-2-yl)-propenone

1-(2-benzyloxy-5-bromophenyl)-3-(6-benzodioxan-1,4-yl)propenone

(2-Benzyloxy-5-bromo-phenyl)-[(2S,3R)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-oxiranyl]-methanone

1-(2-benzyloxy-5-bromophenyl)-3-(6-benzodioxan-1,4-yl)-2,3-epoxypropan-1-one

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