2Fredrick E Behr, Yuri Cheburkov. Minnesota Mining and Manufacturing Company; USA Preparing hydrofluoroethers: WO,9937598 AI[P]. 1999-07-29.
3维维.我国正式加入经修改的《蒙特利尔议定书》.制冷,1991,(2):79-79.
4Krespan Carl G, Rao V N Mallikrjuna. Fluorinated methyl ethers: US,5382704 A[P]. 1995-01-17.
5Dmowski Wojciech, Kolinski RyszardA. Reaction of sulfur tetrafluoride with carboxylic acids. Part IV. Reaction with alkane-dicarboxylic acids[J]. Pol J Chem, 1978,52(1): 71-85.
6Wu kai, Cheng Qingyun. Synthesis of trifluoroethyl ethers from 2,2,2-trifluoroethyl chloride (HCFC-133a) in high temperature aqueous meium[J]. Journal of Fluorine Chemistry, 2002,113(1): 79-83.
7Gubelmann-Bonneau Michel, Poix-Davaine Claire, Ponceblanc Herve. Controlled oxidation of substituted hydrocarbons and heteropoly acid catalysts for use therein: W0,9906338 AI[P]. 1999-02-11.
8Wu Kai, cheng Qingyun. Reaction of HCFC-133a (CF3CH2C1) or HFC-134a (CF3CH2F) with alcohols or phenols in DMSO in the presence of KOH. Chinese Journal of Chemistry, 2001;19(12): 1273-1279.
9John F Olin. Bis(2,2,2-trifluoroethyl)ether: US,3363006[P]. 1968-01-09.
10Wu Kai, Cheng Qingyun. Solvolytically DMSO-promoted reactions of 1,1,1-trifluoroethyl chloride (HCFC-133a) or fluoride (HFC-134a) with nucleophiles [J]. Tetrahedron, 2002,58(20): 4077-4084.
