Reaction of 6-R-8-R?-2,9-Dioxa-1-azabicyclo[4.3.0] nonane derivatives with boron trifluoride etherate

1976 ◽  
Vol 25 (7) ◽  
pp. 1594-1594
Author(s):  
I. E. Chlenov ◽  
Yu. B. Salamonov ◽  
V. A. Tartakovskii
Keyword(s):  
Boron Trifluoride ◽  
Boron Trifluoride Etherate

Synthesis of o-isopentenylphenols

1971 ◽  
Vol 24 (11) ◽  
pp. 2355 ◽  
Author(s):  
J Hlubucek ◽  
E Ritchie ◽  
WC Taylor
Keyword(s):  
Phosphoric Acid ◽  
Zinc Chloride ◽  
Boron Trifluoride ◽  
Boron Trifluoride Etherate ◽  
Stannic Chloride ◽  
Counter Ion

The effect of the solvent and the counter-ion on the ring alkylation of 3- and 4-methoxyphenols by isopentenyl bromide has been examined. Under strictly anhydrous conditions good and consistent yields of the o- isopentenylphenols were obtained with the combination potassium- toluene, but sodium-toluene was more convenient. ��� Boron trifluoride etherate was more satisfactory than stannic chloride, zinc chloride, or phosphoric acid in catalysing the condensation of 3- and 4-methoxy-phenols with 2-methylbut-3-en-2-ol to the corresponding o-isopentenylphenols. Aryl α,α-dimethylpropargyl ethers were partially hydrogenated to the corresponding α,α- dimethylallyl ethers which rearranged in boiling N,N-diethyl-aniline to o-isopentenylphenols in high overall yield.

scholarly journals Synthesis of 5,6,7,8-Tetrahydroquinolines by Thermolysis of Oxime O-Allyl Ethers in the Presence of Boron Trifluoride Etherate.

1993 ◽  
Vol 41 (7) ◽  
pp. 1297-1298 ◽  
Author(s):  
Junko KOYAMA ◽  
Tamaki OGURA ◽  
Kiyoshi TAGAHARA ◽  
Masaaki MIYASHITA ◽  
Hiroshi IRIE
Keyword(s):  
Boron Trifluoride ◽  
Boron Trifluoride Etherate ◽  
Allyl Ethers

Syntheses of the alkali metal borodeuterides

1967 ◽  
Vol 45 (21) ◽  
pp. 2583-2588 ◽  
Author(s):  
J. G. Atkinson ◽  
D. W. MacDonald ◽  
R. S. Stuart ◽  
P. H. Tremaine
Keyword(s):  
Sodium Methoxide ◽  
Boron Trifluoride ◽  
Deuterium Oxide ◽  
Secondary Alcohol ◽  
Boron Trifluoride Etherate ◽  
Residual Hydrogen ◽  
Lithium Deuteride ◽  
Chemical Purity ◽  
Molar Scale ◽  
Sodium Borodeuteride

A synthesis of sodium borodeuteride on a molar scale has been developed. Trimethylamineborane was exchanged (6) with deuteriosulfuric acid in deuterium oxide to obtain trimethylamineborane-d3 of a high isotopic purity. Reaction of trimethylamineborane-d3 with sodium methoxide in diglyme at 120–150 °C yielded sodium borodeuteride, which, after purification, was obtained in a 40–50% overall yield. The conditions for obtaining material of a high isotopic and chemical purity were found to be rather stringent but, once worked out, were easily reproducible.Lithium borodeuteride and potassium borodeuteride were also prepared from trimethylamineborane-d3 and the corresponding methoxide salts. An alternative synthesis of lithium borodeuteride, involving the reaction between lithium deuteride and boron trifluoride etherate, was found to be more satisfactory, since it avoided the formation of stable 1:1 solvent complexes with lithium borodeuteride.The products that were obtained had a chemical purity of 97%, and contained 98–99 atom % deuterium. The deuterium analyses were performed by reducing a series of ketones containing no α hydrogens and analyzing the secondary alcohol by nuclear magnetic resonance for residual hydrogen on the alcohol carbon.

Action of boron trifluoride etherate on unsaturated epoxycompounds

Tetrahedron ◽  
1969 ◽  
Vol 25 (1) ◽  
pp. 1-11 ◽  
Author(s):  
L. Canonica ◽  
M. Ferrari ◽  
U.M. Pagnoni ◽  
F. Pelizzoni ◽  
S. Maroni ◽  
...  
Keyword(s):  
Boron Trifluoride ◽  
Boron Trifluoride Etherate
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