5-Benzoyl-4,7-dichloro-2,3-dihydro-1-benzofuran-2-carboxylic acid

Base Information

• Chemical Name: 5-Benzoyl-4,7-dichloro-2,3-dihydro-1-benzofuran-2-carboxylic acid
• CAS No.: 107804-70-6
• Molecular Formula: C16H10Cl2O4
• Molecular Weight: 337.159
• DSSTox Substance ID: DTXSID40559229

Synonyms:107804-70-6;5-Benzoyl-4,7-dichloro-2,3-dihydro-1-benzofuran-2-carboxylic acid;SCHEMBL10511602;DTXSID40559229;AOEHAAKGUIGREW-UHFFFAOYSA-N;5-benzoyl-4,7-dichloro-2,3-dihydrobenzo[b]furan-2-carboxylic acid

Chemical Property of 5-Benzoyl-4,7-dichloro-2,3-dihydro-1-benzofuran-2-carboxylic acid

Chemical Property:

• XLogP3: 4.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 335.9956142
• Heavy Atom Count: 22
• Complexity: 449

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(OC2=C(C=C(C(=C21)Cl)C(=O)C3=CC=CC=C3)Cl)C(=O)O

Technology Process of 5-Benzoyl-4,7-dichloro-2,3-dihydro-1-benzofuran-2-carboxylic acid

There total 3 articles about 5-Benzoyl-4,7-dichloro-2,3-dihydro-1-benzofuran-2-carboxylic acid 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:

ethyl 5-benzoyl-4,7-dichloro-2,3-dihydrobenzofuran-2-carboxylate → 5-benzoyl-4,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic acid (107804-70-6)

Guidance literature:

With sodium hydroxide; In ethanol; for 2h; Yield given; Heating;

DOI:10.1248/cpb.39.1760

Reference yield:

benzoyl chloride (98-88-4) → 5-benzoyl-4,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic acid (107804-70-6)

Guidance literature:

Multi-step reaction with 2 steps

1: AlCl₃ / 1,2-dichloro-ethane / 1) 0-5 deg C -> r.t., 8 h 2) r.t., overnight

2: 1N NaOH / ethanol / 2 h / Heating

With sodium hydroxide; aluminium trichloride; In ethanol; 1,2-dichloro-ethane;

DOI:10.1248/cpb.39.1760

Reference yield:

ethyl 4,7-dichloro-2,3-dihydrobenzofuran-2-carboxylate (136741-42-9) → 5-benzoyl-4,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic acid (107804-70-6)

Guidance literature:

Multi-step reaction with 2 steps

1: AlCl₃ / 1,2-dichloro-ethane / 1) 0-5 deg C -> r.t., 8 h 2) r.t., overnight

2: 1N NaOH / ethanol / 2 h / Heating

With sodium hydroxide; aluminium trichloride; In ethanol; 1,2-dichloro-ethane;

DOI:10.1248/cpb.39.1760

upstream raw materials:

benzoyl chloride

ethyl 4,7-dichloro-2,3-dihydrobenzofuran-2-carboxylate

Downstream raw materials:

5-chloro-7,8-dihydro-3-phenylfuro<2,3-g>-1,2-benzisoxazole-7-carboxylic acid

4,7-dichloro-2,3-dihydro-5-(α-hydroxyiminobenzyl)benzofuran-2-carboxylic acid

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