Abstract

During the liquid-phase fluorination of 1,1,1-trichloroethane with SbCl 5 · HF, 1,1-dichloroethene is formed. This reacts to give linear and branched oligomers. The hydrolysis of these by-products affords 3,4-dichlorophenol, 6-methyl-4-chloro-2-pyran-2-one and 2- methyl-5,7-dichlorochromone whose source is the acid-catalyzed reaction of water with the trimer and pentamer of 1,1-dichloroethene.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call