ChemInform Abstract: REACTION OF PHOSPHORUS PENTACHLORIDE WITH IMIDOYLAMIDINES

1978 ◽  
Vol 9 (45) ◽  
Author(s):  
P. P. KORNUTA ◽  
N. V. KOLOTILO
1982 ◽  
Vol 13 (42) ◽  
Author(s):  
S. V. FRIDLAND ◽  
I. A. SHKURAI ◽  
L. I. LAPTEVA

1978 ◽  
Vol 9 (22) ◽  
Author(s):  
M. A. KAZANKOVA ◽  
T. YA. SATINA ◽  
V. D. LUN'KOV ◽  
I. F. LUTSENKO

1975 ◽  
Vol 12 (1) ◽  
pp. 219-220 ◽  
Author(s):  
Gerald A. Poulton ◽  
Mary E. Williams

Langmuir ◽  
2017 ◽  
Vol 33 (35) ◽  
pp. 8766-8773 ◽  
Author(s):  
Muhammad Amirul Islam ◽  
Md Hosnay Mobarok ◽  
Regina Sinelnikov ◽  
Tapas K. Purkait ◽  
Jonathan G. C. Veinot

1976 ◽  
Vol 7 (21) ◽  
pp. no-no
Author(s):  
A. F. KOLOMIETS ◽  
A. V. FOKIN ◽  
A. A. KROLEVETS ◽  
O. V. BRONNYI

1978 ◽  
Vol 9 (51) ◽  
Author(s):  
A. V. FOKIN ◽  
A. F. KOLOMIETS ◽  
A. A. KROLEVETS

1973 ◽  
Vol 51 (12) ◽  
pp. 2017-2023 ◽  
Author(s):  
E. Wilkins Reeve ◽  
Thomas F. Steckel

Reactions of phosphorus pentachloride with ethyl(trichloromethyl)carbinol (2), (trichloromethyl)-vinylcarbinol (7), ethynyl(trichloromethyl)carbinol (11a), and 1,1,1-trichloro-3-nonyn-2-ol (11b) have been studied. Whereas the reaction of phenyl(trichloromethyl)carbinol with phosphorus pentachloride leads to a nearly quantitative replacement of the hydroxyl group by chlorine, the reactions of the aliphatic (trichloromethyl)carbinols are more complicated. Thus the reaction of 2 with phosphorus pentachloride gave 18% of the normal product, 1,1,1,2-tetrachlorobutane (3), 13% of 1,1,2-trichloro-1-butene (4) from a dehydrohalogenation, and a higher boiling phosphate ester – acid chloride mixture. The alkynylcarbinols (11) gave tetrachlorobutynes (12) as well as tetrachloroallenes (13) by allylic rearrangement. A crystalline phosphate ester of 11a was also isolated. Several examples are given of catalytic rearrangements in the vapor phase of 1,1,1-trichloro-2-alkenes to 1,1,3-trichloro-1-alkenes.


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