1318760-01-8

Basic information

• Product Name: 6-(benzo[d][1,3]dioxol-5-yl)-2-phenyl-2,3,6,7-tetrahydrobenzofuran-4(5H)-one
• Synonyms: 6-(benzo[d][1,3]dioxol-5-yl)-2-phenyl-2,3,6,7-tetrahydrobenzofuran-4(5H)-one
• CAS NO: 1318760-01-8
• Molecular Weight: 334.372
• Mol File: 1318760-01-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-(benzo[d][1,3]dioxol-5-yl)-2-phenyl-2,3,6,7-tetrahydrobenzofuran-4(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(benzo[d][1,3]dioxol-5-yl)-2-phenyl-2,3,6,7-tetrahydrobenzofuran-4(5H)-one(1318760-01-8)
• EPA Substance Registry System: 6-(benzo[d][1,3]dioxol-5-yl)-2-phenyl-2,3,6,7-tetrahydrobenzofuran-4(5H)-one(1318760-01-8)

Safety Data

• Hazardous Substances Data: 1318760-01-8(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 1318759-84-0 5-(benzo[d]-[1,3]dioxo-5-yl)-2-diazohexane-1,3-dione 

Relevant articles and documents

One-pot Synthesis of Dihydrofuran Derivatives by Ru Catalyzed Reaction

The present invention relates to a one-pot synthesis method of dihydrofuran derivatives using a ruthenium catalyst and, more particularly, to a one-pot synthesis method of dihydrofuran derivatives, which makes a reaction between cyclic/non-cyclic diazo dicarbonyl compound and olefin in the presence of ruthenium (II) phosphine complex as a reaction catalyst. The one-pot synthesis method of the present invention shortens time required for the reaction and improves synthesis yield. The diazo carbonyl compound represented by chemical formula 1, 2, or 3 reacts with olefin to form dihydrofuran derivatives through a [3+2] cyclization addition reaction.COPYRIGHT KIPO 2016

AgBF4/[Bmim]BF4-Catalyzed [3+2] cycloaddition of cyclic diazodicarbonyl compounds: Efficient synthesis of 2,3-dihydrofurans and conversion to 3-acylfurans

A novel and efficient method for the synthesis of 2,3-dihydrofurans bearing a variety of substituents on the dihydrofuran ring was achieved by the reaction of cyclic diazodicarbonyl compounds with styrene and vinyl acetate. The key strategy was AgBF4