Ethyl 2-(3-bromophenoxy)acetate

Base Information

• Chemical Name: Ethyl 2-(3-bromophenoxy)acetate
• CAS No.: 138139-14-7
• Molecular Formula: C10H11BrO3
• Molecular Weight: 259.1
• Hs Code.: 2918990090
• DSSTox Substance ID: DTXSID70409389
• Wikidata: Q82215206
• Mol file: 138139-14-7.mol

Synonyms:Ethyl 2-(3-bromophenoxy)acetate;138139-14-7;ethyl (3-bromophenoxy)acetate;(3-BROMOPHENOXY) ACETIC ACID ETHYL ESTER;(3-Bromophenoxy)acetic acid ethyl ester;ethyl 3-bromophenyloxyacetate;ethyl 3-bromophenoxyacetate;SCHEMBL7033340;Ethyl2-(3-bromophenoxy)acetate;DTXSID70409389;SOKSJIDLQWRXTN-UHFFFAOYSA-N;MFCD03945182;AKOS003324421;AB16880;FS-4132;(3-BROMOPHENOXY)ACETICACIDETHYLESTER;CS-0211625;EN300-60435;D78582;A886303;Z53835270

Chemical Property of Ethyl 2-(3-bromophenoxy)acetate

Chemical Property:

• PSA: 35.53000
• LogP: 2.39100
• Storage Temp.: Room temperature.
• XLogP3: 2.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 257.98916
• Heavy Atom Count: 14
• Complexity: 184

Purity/Quality:

97% ^*data from raw suppliers

Ethyl2-(3-bromophenoxy)acetate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC(=O)COC1=CC(=CC=C1)Br

Technology Process of Ethyl 2-(3-bromophenoxy)acetate

There total 3 articles about Ethyl 2-(3-bromophenoxy)acetate 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: 95.5%

3-Bromophenol (591-20-8) + ethyl bromoacetate (105-36-2) → ethyl 3-bromophenyloxyacetate (138139-14-7)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

Reference yield: 77.0%

3-Bromophenol (591-20-8) + chloroacetic acid ethyl ester (105-39-5) → ethyl 3-bromophenyloxyacetate (138139-14-7)

Guidance literature:

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

DOI:10.1016/j.bmc.2010.11.034

Reference yield:

→ ethyl 3-bromophenyloxyacetate (138139-14-7)

Guidance literature:

upstream raw materials:

3-Bromophenol

ethyl bromoacetate

chloroacetic acid ethyl ester

Downstream raw materials:

3-bromophenoxyacetic acid

1-bromo-3-(fluoromethoxy)benzene

[(2'-methoxybiphenyl-3-yl)oxy]acetic acid