278611-73-7

Basic information

• Product Name: tert-butyl 2-[N-(p-methoxyphenyl)imino]-3,3,3-trifluoropropanoate
• Synonyms: tert-butyl 2-[N-(p-methoxyphenyl)imino]-3,3,3-trifluoropropanoate
• CAS NO: 278611-73-7
• Molecular Weight: 303.281
• Mol File: 278611-73-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl 2-[N-(p-methoxyphenyl)imino]-3,3,3-trifluoropropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 2-[N-(p-methoxyphenyl)imino]-3,3,3-trifluoropropanoate(278611-73-7)
• EPA Substance Registry System: tert-butyl 2-[N-(p-methoxyphenyl)imino]-3,3,3-trifluoropropanoate(278611-73-7)

Safety Data

• Hazardous Substances Data: 278611-73-7(Hazardous Substances Data)

Upstream product

• 201230-82-2 carbon monoxide 
• 134481-27-9 N-(4-methoxyphenyl)-2,2,2-trifluoroacetimidoyl iodide 
• 75-65-0 tert-butyl alcohol 

Downstream Products

• 278611-80-6 tert-butyl 2-[N-(p-methoxyphenyl)amino]-2-trifluoromethyl-4-pentenoate 
• 278611-79-3 tert-butyl 2-phenyl-2-[N-(p-methoxyphenyl)amino]-3,3,3-trifluoropropanoate 
• 278611-81-7 tert-butyl 6-phenyl-2-[N-(p-methoxyphenyl)amino]-2-trifluoromethyl-5-hexynoate 
• 278611-78-2 tert-butyl 2-[N-(p-methoxyphenyl)amino]-2-trifluoromethylhexanoate 

Relevant articles and documents

Preparation, structure, and reactions of trifluoroacetimidoyl palladium(II) complexes

Trifluoroacetimidoyl metal complexes are useful intermediates for the selective synthesis of organofluorine compounds. Herein, we report preparations, structures, and reactions of fluorinated imidoyl palladium complexes. Oxidative addition of trifluoroacetimidoyl halides to Pd(PPh3)4 afforded quantitatively the imidoyl palladium(II) complexes with phosphine ligands. The reaction of trifluoroacetimidoyl iodides with Pd 2(dba)3 provided the phosphine-free imidoyl palladium complex in high yields. The X-ray crystal structure analysis of the phosphine-free complex [Pd(μ-I){μ-C(CF3)=N(PMP)}]4 revealed a cyclic tetranuclear structure containing the imidoyl and iodo bridges. The generation of aminotrifluoromethylcarbene equivalents by protonation or electrophilic alkylation of imidoyl palladium(II) complexes is discussed.