1402010-78-9

Basic information

• Product Name: 3-(1-(benzyloxy)-3-phenylpropyl)thiophene
• Synonyms: 3-(1-(benzyloxy)-3-phenylpropyl)thiophene
• CAS NO: 1402010-78-9
• Molecular Weight: 308.444
• Mol File: 1402010-78-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(1-(benzyloxy)-3-phenylpropyl)thiophene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1-(benzyloxy)-3-phenylpropyl)thiophene(1402010-78-9)
• EPA Substance Registry System: 3-(1-(benzyloxy)-3-phenylpropyl)thiophene(1402010-78-9)

Safety Data

• Hazardous Substances Data: 1402010-78-9(Hazardous Substances Data)

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 1402010-12-1 potassium (1-hydroxy-3-phenylpropyl)trifluoroboranuide 
• 17249-80-8 3-chlorothiophene 
• 1402010-11-0 potassium (1-benzyloxy-3-phenylpropyl)trifluoroboranuide 
• 100-39-0 benzyl bromide 

Relevant articles and documents

Stereospecific cross-coupling of secondary organotrifluoroborates: Potassium 1-(benzyloxy)alkyltrifluoroborates

Potassium 1-(alkoxy/acyloxy)alkyltrifluoroborates have been synthesized through a copper-catalyzed diboration of aldehydes and subsequent conversion of the resulting potassium 1-(hydroxy)alkyltrifluoroborates. The palladium-catalyzed Suzuki-Miyaura reaction employing the potassium 1-(benzyloxy)alkyltrifluoroborates with aryl and heteroaryl chlorides provides access to protected secondary alcohols in high yields. The β-hydride elimination pathway is avoided through use of the benzyl protecting group, which is proposed to stabilize the diorganopalladium intermediate by coordination of the arene to the metal center. This cross-coupling is stereospecific with complete retention of stereochemistry.