156203-61-1

Basic information

• Product Name: 3,3-Diphenyl-tetrahydro-furan-2-ol
• Synonyms: 3,3-Diphenyl-tetrahydro-furan-2-ol
• CAS NO: 156203-61-1
• Molecular Weight: 240.302
• Mol File: 156203-61-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3,3-Diphenyl-tetrahydro-furan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3-Diphenyl-tetrahydro-furan-2-ol(156203-61-1)
• EPA Substance Registry System: 3,3-Diphenyl-tetrahydro-furan-2-ol(156203-61-1)

Safety Data

• Hazardous Substances Data: 156203-61-1(Hazardous Substances Data)

Upstream product

• 956-89-8 3,3-Diphenyl-dihydro-furan-2-one 
• 3468-99-3 ethyl diphenylacetate 

Downstream Products

• 127527-61-1 2-methoxy-3,3-diphenyltetrahydrofuran 
• 1427003-07-3 3-butyl-5,5-diphenyl-6,7-dihydrooxepin-2(5H)-one 
• 898528-50-2 allyl-(3,3-diphenyl-pent-4-enyl)-carbamic acid benzyl ester 
• 898528-56-8 4,4-diphenyl-2,3,4,7-tetrahydro-azepine-1-carboxylic acid benzyl ester 
• 898528-46-6 allyl-(3,3-diphenyl-pent-4-enyl)-amine 
• 162466-82-2 3,3-diphenyl-4-penten-1-ol 
• 69177-62-4 3,3-Diphenyl-tetrahydro-furan 

Relevant articles and documents

Catalytic method for the reduction of lactones to lactols

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A new strategy for efficient synthesis of medium and large ring lactones without high dilution or slow addition

We have developed an efficient method for medium and large ring lactone synthesis by a conceptually different ring-expansion strategy. The design of an unprecedented ring conjunction mode of oxetene, combined with the appropriate choice of a Lewis acid promoter and an additive, constitutes the key components of the new process. Enabled by this new approach, the reaction does not require high dilution or slow addition.

Convenient Two-Step Conversion of Lactones into Cyclic Ethers

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