369-54-0Relevant articles and documents
Microwave-assisted synthesis of 1,4-bis(difluoromethyl)benzene
Pan, Dong-Hui,Wang, Tong-Zhen,Xiao, Guo-Min
, p. 1249 - 1254 (2017)
A fast, mild, and practical microwave-assisted protocol for synthesis of 1,4-bis(difluoromethyl)benzene from 1,4-bis(dichloromethyl)benzene and KF was developed. The new protocol increased the yield and reduced the reaction time significantly in contrast to the conventional heating procedure. Also, the synergistic effect of a composite phase transfer catalyst was studied.
Direct Difluoromethylation of Aryl Halides via Base Metal Catalysis at Room Temperature
Xu, Long,Vicic, David A.
supporting information, p. 2536 - 2539 (2016/03/12)
A stable and isolable difluoromethyl zinc reagent has been prepared through the reaction of ICF2H with diethyl zinc and DMPU. This new zinc reagent is a free-flowing solid and can be used in combination with a nickel catalyst to difluoromethylate aryl iodides, bromides, and triflates at room temperature. Such mild conditions for the catalytic difluoromethylation of these substrates are unprecedented.
Efficient synthesis of p-bis-(chlorodifluoromethyl)benzene
Dolbier Jr., William R.,Duan, Jian-Xin,Rong, Xiao X.
, p. 1091 - 1093 (2008/02/08)
Selective, high yield partial fluorination of p-bis-(trichloromethyl)benzene to p-bis-(chlorodifluoromethyl)benzene has been accomplished by warming a slurry of the p-bis-(trichloromethyl)benzene in anhydrous HF which also contains a small quantity of inert solvent, such as 1,2-dichloroethane.