2431-50-7Relevant articles and documents
Transmetallation of β-allenyl silanes: Efficient synthesis of dienyl chlorostannanes and chlorostibines
Lahrech, Mokhtar,Thibonnet, Jerome,Hacini, Salih,Santelli, Maurice,Parrain, Jean-Luc
, p. 644 - 645 (2002)
The reaction of 1-trimethylsilylbuta-2,3-diene with tin tetrachloride, antimony trichloride or antimony pentachloride gave the corresponding buta-1,3-dien-2-yl halostannane or stibine derivatives; this ligand exchange was extended to other β-allenylsilane
Chlorination of chloroolefins C3-C4
Levanova,Strizhakova,Sokolov,Aseev,Lapidus
, p. 255 - 257 (2007/10/03)
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CHEMISTRY OF DIENES AND THEIR DERIVATIVES. XVII. LOW-TEMPERATURE CHLORINATION OF 2-CHLORO- AND 1,2-DICHLORO-1,3-BUTADIENES IN THE PRESENCE OF AN INHIBITOR OF RADICAL REACTIONS
Mkryan, G. M.,Airapetyan, R. Kh.,Mkryan, G. G.,Kaplanyan, E. E.
, p. 1242 - 1247 (2007/10/02)
During the chlorination of chloroprene (80-85percent conversion) in carbon tetrachloride at -5 to 0 deg C in the presence of tert-butylpyrocatechol 1,2-dichloro-1,3-butadiene, 3,3,4-trichloro-1-butene, 2,3,4-trichloro-1-butene, and 1,2,4-trichloro-2-butene are formed in percentage ratios of 20.4:6.7:3.4:69.5.During chlorination to total conversion of chloroprene under these conditions a series of other compounds are also formed as a result of the further chlorination of 1,2-dichloro-1,3-butadiene and 3,3,4-trichloro-1-butene.During the chlorination of 1,2-dichloro-1,3-butadiene to a high degree of conversion 1,2,4-trichloro-1,3-butadiene, 1,2,3,4-tetrachloro-1-butene, and 1,1,2,4-tetrachloro-2-butene are formed in ratios of 11.4:49:39.6.