Ethyl ((3-amino-2-benzoyl-1-benzofuran-7-YL)oxy)acetate

Base Information

Chemical Name:Ethyl ((3-amino-2-benzoyl-1-benzofuran-7-YL)oxy)acetate
CAS No.:301538-61-4
Molecular Formula:C₁₉H₁₇NO₅
Molecular Weight:339.348
Hs Code.:
European Community (EC) Number:669-002-2

Synonyms:301538-61-4;Ethyl 2-((3-amino-2-benzoylbenzofuran-7-yl)oxy)acetate;ETHYL ((3-AMINO-2-BENZOYL-1-BENZOFURAN-7-YL)OXY)ACETATE;AKOS024321089

Suppliers and Price of Ethyl ((3-amino-2-benzoyl-1-benzofuran-7-YL)oxy)acetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Ethyl ((3-amino-2-benzoyl-1-benzofuran-7-YL)oxy)acetate

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:7
Exact Mass:339.11067264
Heavy Atom Count:25
Complexity:476

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)COC1=CC=CC2=C1OC(=C2N)C(=O)C3=CC=CC=C3

Technology Process of Ethyl ((3-amino-2-benzoyl-1-benzofuran-7-YL)oxy)acetate

There total 2 articles about Ethyl ((3-amino-2-benzoyl-1-benzofuran-7-YL)oxy)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: 91.0%

: 105-36-2
ethyl bromoacetate

: 301538-51-2
3-Amino-2-benzoyl-1-benzofuran-7-ol

: 301538-61-4
Ethyl [(3-amino-2-benzoyl-1-benzofuran-7-yl)oxy]acetate

Guidance literature:: With potassium carbonate; In butanone; for 12h; Heating;
DOI:10.1135/cccc20001093

Reference yield:

: 269075-50-5
2-Benzoyl-7-methoxy-1-benzofuran-3-amine

: 301538-61-4
Ethyl [(3-amino-2-benzoyl-1-benzofuran-7-yl)oxy]acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 42 percent / BBr₃ / CH₂Cl₂ / 7 h / 20 °C

2: 91 percent / K₂CO₃ / butan-2-one / 12 h / Heating

With boron tribromide; potassium carbonate; In dichloromethane; butanone; 1: Ether cleavage; Demethylation / 2: Etherification;
DOI:10.1135/cccc20001093