1-(5-Hydroxy-2-methyl-1-benzofuran-3-yl)ethanone

Base Information

• Chemical Name: 1-(5-Hydroxy-2-methyl-1-benzofuran-3-yl)ethanone
• CAS No.: 28241-99-8
• Molecular Formula: C11H10O3
• Molecular Weight: 190.1953
• Hs Code.: 2932999099
• DSSTox Substance ID: DTXSID60354637
• Nikkaji Number: J544.050E
• Wikidata: Q82132896
• Mol file: 28241-99-8.mol

Synonyms:28241-99-8;1-(5-hydroxy-2-methyl-1-benzofuran-3-yl)ethanone;1-(5-Hydroxy-2-methylbenzofuran-3-yl)ethanone;3-acetyl-5-hydroxy-2-methylbenzofuran;1-(5-Hydroxy-2-methyl-benzofuran-3-yl)-ethanone;1-(5-Hydroxy-2-methyl-1-benzofuran-3-yl)ethan-1-one;1-(5-hydroxy-2-methylbenzofuran-3-yl)ethan-1-one;104260-72-2;Ethanone,1-(5-hydroxy-2-methyl-3-benzofuranyl)-;DTXSID60354637;2-(Acetamidobenzylidene)malononitrile;BBL025693;MFCD00464117;STL360573;AKOS000267128;VS-08055;CS-0072956;FT-0682985;UNM000011039401;D83355;EN300-240210;1-(5-Hydroxy-2-methyl-3-benzofuranyl)-ethanone;A876759;Z57082103;F1387-0005

Chemical Property of 1-(5-Hydroxy-2-methyl-1-benzofuran-3-yl)ethanone

Chemical Property:

• Melting Point: 238℃
• Boiling Point: 344 °C at 760 mmHg
• Flash Point: 161.9 °C
• PSA: 50.44000
• Density: 1.246 g/cm³
• LogP: 2.64940
• Storage Temp.: 2-8°C
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 190.062994177
• Heavy Atom Count: 14
• Complexity: 239

Purity/Quality:

97% ^*data from raw suppliers

1-(5-hydroxy-2-methyl-1-benzofuran-3-yl)ethanone ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C2=C(O1)C=CC(=C2)O)C(=O)C

Technology Process of 1-(5-Hydroxy-2-methyl-1-benzofuran-3-yl)ethanone

There total 10 articles about 1-(5-Hydroxy-2-methyl-1-benzofuran-3-yl)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: 70.0%

(E)-4-(phenylamino)pent-3-en-2-one (147054-81-7) + p-benzoquinone (106-51-4) → 1-(5-hydroxy-2-methylbenzofuran-3-yl)ethan-1-one (28241-99-8) + 1-(5-hydroxy-2-methyl-1-phenyl-1H-indol-3-yl)ethanone (5102-18-1)

Guidance literature:

In 1,2-dichloro-ethane; Ambient temperature;

DOI:10.1007/BF00781075

Reference yield: 58.0%

(E)-4-amino-pent-3-en-2-one (80012-14-2) + p-benzoquinone (106-51-4) → 2-methyl-3-acetyl-5-hydroxyindole (57827-05-1) + 1-(5-hydroxy-2-methylbenzofuran-3-yl)ethan-1-one (28241-99-8)

Guidance literature:

With acetic acid; Ambient temperature;

DOI:10.1007/BF00781075

Reference yield: 53.0%

4-methylaminopent-3-en-2-one (130256-90-5) + p-benzoquinone (106-51-4) → 1-(5-hydroxy-2-methylbenzofuran-3-yl)ethan-1-one (28241-99-8) + 1-(5-hydroxy-1,2-dimethyl-1H-indol-3-yl)ethanone (135333-93-6)

Guidance literature:

With acetic acid; Ambient temperature;

DOI:10.1007/BF00781075

upstream raw materials:

pyridine

acetylacetone

p-benzoquinone

4-amino-3-penten-2-one

Downstream raw materials:

1-(5-methoxy-2-methylbenzofuran-3-yl)ethanone

1-[5-(4-bromobenzyloxy)-2-methylbenzofuran-3-yl]ethanone