29778-28-7

Basic information

• Product Name: 1-FLUORO-3-(2-PHENYLETHYNYL)BENZENE
• Synonyms: 1-FLUORO-3-(2-PHENYLETHYNYL)BENZENE
• CAS NO: 29778-28-7
• Molecular Formula: C₁₄H₉F
• Molecular Weight: 196.22
• Mol File: 29778-28-7.mol
• Article Data: 26

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-FLUORO-3-(2-PHENYLETHYNYL)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-FLUORO-3-(2-PHENYLETHYNYL)BENZENE(29778-28-7)
• EPA Substance Registry System: 1-FLUORO-3-(2-PHENYLETHYNYL)BENZENE(29778-28-7)

Safety Data

• Hazardous Substances Data: 29778-28-7(Hazardous Substances Data)

Upstream product

• 13146-23-1 copper(I) phenylacetylenide 
• 1121-86-4 1-Fluoro-3-iodobenzene 
• 536-74-3 phenylacetylene 
• 1073-06-9 3-fluorobromobenzene 
• 591-50-4 iodobenzene 
• 52776-46-2 1-fluoro-2-phenylacetylene 
• 2561-17-3 1-ethynyl-3-fluoro-benzene 
• 369-57-3 benzenediazonium tetrafluoroborate 
• 62-53-3 aniline 
• 16635-23-7 phenyltriisopropoxytitanium(IV) 
• 813414-83-4 1-bromo-2-(meta-fluorophenyl)ethyne 
• 100-44-7 benzyl chloride 
• 4706-43-8 1-benzyl-1H-benzotriazole 
• 456-48-4 3-Fluorobenzaldehyde 

Downstream Products

• 3834-65-9 1-(3-fluorophenyl)-2-phenylethane-1,2-dione 
• 1437733-33-9 (Z)-3-(2-(3-fluorophenyl)-1-phenylvinyl)-1,2,4,5-tetramethylbenzene 
• 19466-30-9 (E)-3-fluorostilbene 
• 19466-30-9 (Z)-1-fluoro-3-styrylbenzene 
• 144054-13-7 2-(3-fluorophenyl)-3-phenyl-1H-indole 

Relevant articles and documents

A facile protocol for copper-free palladium-catalyzed Sonogashira coupling in aqueous media

The combination of a readily available palladium catalyst and an eco-friendly basic aqueous solution of room-temperature ionic liquid, choline hydroxide (ChOH), was used in a facile protocol alternative to the Sonogashira coupling reaction, alkynylation of aryl halides in the absence of a copper cocatalyst and an external base. The dual nature of ChOH to act as a base and a green solvent played a crucial role in the catalytic cycle. The coupling reaction progressed efficiently to form a Csp-Csp2 bond under the identified conditions although the reaction outcome depended significantly on the substrates.

Facile one-pot synthesis of diarylacetylenes from arylaldehydes: Via an addition-double elimination process

A practical one-pot protocol has been developed to synthesize diarylacetylenes from arylaldehydes by treatment with 1-(arylmethyl)benzotriazoles and LiN(SiMe3)2. The reaction proceeded through imine formation, Mannich-type addition and double elimination to deliver products in up to 99% yields with broad substrate scope. In addition, gram-scale synthesis of 1-bromo-4-(phenylethynyl)benzene has been demonstrated.

Simple and efficient diaryl alkyne synthesis method

The embodiment of the invention discloses a simple and efficient diaryl alkyne synthesis method. The method comprises the steps of by taking arylmethylbenzotriazole and aromatic aldehyde as raw materials, carrying out addition and double-beta-elimination reaction under the action of bis (trimethylsilyl) amino salt MN (SiMe3) 2 to synthesize diaryl alkyne by a one-pot method. The raw materials and chemical reagents used in the method are easy to obtain, the reaction conditions are mild, the operation is simple, the substrate universality is good, the product yield is high, and the method is a simple and efficient diaryl alkyne synthesis method.