420-25-7Relevant academic research and scientific papers
A method for the preparation of ethylene fluorine bromine
-
Paragraph 0036; 0037, (2017/05/02)
The invention discloses a preparation method of 1-bromo-1-fluoroethylene.The preparation method comprises: two-stage bromination reaction and hydrogen bromide removal reaction; and has the characteristics of easily-available raw materials, low temperature of hot bromination reactions, high reaction yield, low cost, green, and environment-friendliness.
Method for producing 1,1-dibromo-1-fluoroethane
-
Paragraph 0124; 0125, (2016/11/21)
The present invention addresses the problem of providing a production method which enables 1,1-dibromo-1-fluoroethane to be produced in a simple and sustained manner. The present invention provides a method for producing 1,1-dibromo-1-fluoroethane, said method comprising step A of reacting 1,1-dibromoethylene with hydrogen fluoride to produce 1,1-dibromo-1-fluoroethane.
METHOD FOR PRODUCING 1,1-DIBROMO-1-FLUOROETHANE
-
Paragraph 0089, (2016/08/29)
An object of the present invention is to provide a production method that makes it possible to produce 1,1-dibromo-1-fluoroethane easily and sustainably. The present invention provides a method for producing 1,1-dibromo-1-fluoroethane, the method comprising step A of reacting 1,1-dibromoethylene with hydrogen fluoride to obtain 1,1-dibromo-1-fluoroethane.
PRODUCTION METHOD OF MONOFLUOROETHYLENE COMPOUND
-
Paragraph 0033, (2016/12/22)
PROBLEM TO BE SOLVED: To provide a synthesis method capable of giving a monofluoroethylene compound with a difluoroethylene compound as a material, under mild conditions, at ease and with high selectivity. SOLUTION: A production method of a monofluoroethylene compound represented by the formulas (1-1), (1-2) or (1-3) comprises a step of a difluoroethylene compound represented by the formulas (2-1), (2-2) or (2-3) with a compound represented by the formula (3): BX3, to obtain a monofluoroethylene compound represented by the formulas (1-1), (1-2) or (1-3). [R1 and R2 may be identically or differently H, an alkyl group, or a phenyl group which may be substituted with one or more substituent groups, or may be linked to each other to form a carbocyclic ring; and X is Cl or Br.] COPYRIGHT: (C)2015,JPOandINPIT
Low-temperature 19F NMR spectroscopy of 1-fluoro-1-lithioethenes - Stability, shifts and unexpected coupling constants
Kvicala, Jaroslav,Hrabal, Richard,Czernek, Jiri,Bartosova, Ivana,Paleta, Oldrich,Pelter, Andrew
, p. 211 - 218 (2007/10/03)
Half-lives and fluorine atom shifts of stabilized 1-fluoro-l-lithioethenes bearing hydrogen, fluorine, phenyl, and/or dimethylphenylsilyl groups in the β-positions have been determined by a low-temperature 19F NMR spectroscopy. Some 1-fluoro-1-lithioethenes displayed an exceptionally low value of the trans-3JFF coupling constant. Stereoselectivity of carbenoid formation, as well as an effect of configuration on the stability is discussed.
Vibrational Excitation of the Reaction between Vinyl Bromide and Fluorine in Solid Argon
Cesaro, Stella Nunziante,Frei, Heinz,Pimentel, George C.
, p. 2142 - 2147 (2007/10/02)
A number of unsuccessful attempts to induce bimolecular addition reactions with selective vibrational excitation in cryogenic solids are reported here: 1,3-butadiene with Cl2, ClF, Br2, I2, and XeF2; vinyl chloride with F2.One system, vinyl bromide with fluorine in solid argon, did respond by showing reaction product growth upon laser excitation at 3116, 3098, 1849, 1808, and 1605 cm-1.Identification of reaction products suggests F2 addition across the double bond followed significantly by HF elimination but apparently without HBr elimination.Relative quantum yields display a monotonic dependence upon photon energy that is even more dramatic than that found earlier for the ethylene-fluorine reaction.Thus excitation of the C-H stretching modes either at 3116 or 3098 cm-1 is 102 times more effective than excitation at 1849 or 1848 cm-1 and 103 times more effective than at 1605 cm-1.
