3801-53-4

Basic information

• Product Name: Benzene, 1-chloro-4-[(4-fluorophenyl)methyl]-
• CAS NO: 3801-53-4
• Molecular Formula: C13H10ClF
• Molecular Weight: 220.674
• Mol File: 3801-53-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-4-[(4-fluorophenyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-4-[(4-fluorophenyl)methyl]-(3801-53-4)
• EPA Substance Registry System: Benzene, 1-chloro-4-[(4-fluorophenyl)methyl]-(3801-53-4)

Safety Data

• Hazardous Substances Data: 3801-53-4(Hazardous Substances Data)

Upstream product

• 873-77-8 (4-chlorphenyl)magnesium bromide 
• 462-06-6 fluorobenzene 
• 1352918-92-3 N-((4-chlorobenzyl)oxy)-N-methylacetamide 
• 459-56-3 4-fluorobenzylic alcohol 
• 1679-18-1 4-Chlorophenylboronic acid 
• 104-88-1 4-chlorobenzaldehyde 
• 459-57-4 4-fluorobenzaldehyde 
• 1765-93-1 4-fluoroboronic acid 
• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 2795-76-8 4-chloro-α-(4-fluorophenyl)benzenemethanol 
• 460-00-4 1-Bromo-4-fluorobenzene 
• 6332-83-8 2-(4-chlorophenyl)-1-phenylethanone 

Relevant articles and documents

Alumina grafted SBA-15 sustainable bifunctional catalysts for direct cross-coupling of benzylic alcohols to diarylmethanes

AlSBA-15 catalysts possessing Br?nsted acid and Lewis acid-base bifunctionalities catalyze the direct arylation of benzyl alcohols to diarylmethanes with an 85% product yield through C-O bond activation. 2 and 4wt%AlSBA-15 catalysts have been synthesised by adopting a simple and efficient post-synthetic metal implantation route. The synthesised catalysts were characterized using XRD, N2 adsorption and desorption, 27Al MAS NMR, XPS, HR-TEM, NH3 and CO2-temperature-programmed desorption (TPD) and pyridine-transmission-FTIR spectroscopy techniques to confirm the existence of Br?nsted acid and Lewis acid-base bifunctionalities. Through various control experiments, it is verified that Br?nsted acid sites activate the benzyl alcohol and Lewis base sites interact with phenylboronic acid concurrently to accomplish the coupling reaction. In the recyclability study, 4wt%AlSBA-15 preserves its activity and stability up to 5 cycles. The 4wt%AlSBA-15 catalyst unlike homogeneous catalysts does not require additives, long reaction time and expensive metals.

Palladium-catalyzed synthesis of diarylmethanes: Exploitation of carbanionic leaving groups

A novel route to the synthesis of diarylmethanes via a Pd-catalyzed α-arylation of benzyl ketones is rseported. By harnessing the inherent reactivity of enolates, it is possible to circumvent the need for a transmetalating reagent such as boron for the co

Preparation process of fluorine substituted aromatic compound

A preparation process of a fluorine substituted aromatic compound comprising reacting an alkali metal or alkali earth metal salt of an aromatic compound having a hydroxy group with an organic fluorinating agent is disclosed. As a representative fluorinating agent, a bis-dialkylamino-difluoromethane compound, for example, 2,2′-difluoro-1,3-dimethylimidazolidine, is exemplified. According to the process, an industrially useful fluorinated aromatic compound, for example, a fluorobenzene, a fluorine substituted benzophenone, a fluorine substituted diarylsulfone can be prepared with ease in economy without specific equipment.