1410747-77-1

Basic information

• Product Name: tert-butyl benzyl(2,3-dihydrobenzofuran-3-yl)carbamate
• Synonyms: tert-butyl benzyl(2,3-dihydrobenzofuran-3-yl)carbamate
• CAS NO: 1410747-77-1
• Molecular Weight: 325.408
• Mol File: 1410747-77-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl benzyl(2,3-dihydrobenzofuran-3-yl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl benzyl(2,3-dihydrobenzofuran-3-yl)carbamate(1410747-77-1)
• EPA Substance Registry System: tert-butyl benzyl(2,3-dihydrobenzofuran-3-yl)carbamate(1410747-77-1)

Safety Data

• Hazardous Substances Data: 1410747-77-1(Hazardous Substances Data)

Upstream product

• 109926-35-4 dihydro-2,3 benzofurannamine-3 
• 82415-84-7 benzofuran-3(2H)-one oxime 
• 1410747-74-8 tert-butyl (2,3-dihydrobenzofuran-3-yl)carbamate 
• 100-39-0 benzyl bromide 
• 1410747-80-6 tert-butyl N-(tert-butoxycarbonyl)-(2,3-dihydrobenzofuran-3-yl)carbamate 

Downstream Products

• 1410748-15-0 N-benzyl-2,3-dihydrobenzofuran-3-amine 

Relevant articles and documents

Lewis-acid-mediated ring-exchange reaction of dihydrobenzofurans and its application to the formal total synthesis of (-)-quinocarcinamide

An unusual Lewis-acid-mediated ring-exchange reaction of dihydrobenzofurans is described. The fused tricyclic ring system is the key structural element for this reaction as it restricts C-N bond rotation and/or destabilizes the benzofuran ring. We achieved the formal total synthesis of (-)-quinocarcinamide using a combination of this reaction and the Au(I)-catalyzed 6-endo-dig hydroamination of an alkyne.