Boron trifluoride etherate → Nonane

For example, the appropriate lithium trisubstituted-silylacetylene (2) is contacted with an equimolar amount of B-methoxy-9-borabicyclo[3.3.1]nonane (3) in a suitable anhydrous inert organic solvent such as tetrahydrofuran, hexane, t-butyl methyl ether, diethyl ether, pentane and the like with tetrahydrofuran being preferred. The reactants are typically stirred together under an inert atmosphere for a period of time ranging from 5 minutes to 48 hours at a temperature range of from -78° C. to room temperature. A temperature range of -78° C. to -40° C. and a reaction time of 1.5 hours to 5 hours are preferred. The intermediate "ate" complex thus formed is contacted with a molar excess of a suitable lewis acid such as boron trifluoride etherate, boron trichloride and the like with boron trifluoride etherate being preferred. The reactants are typically stirred together under an inert atmosphere for a period of time ranging from 5 minutes to 24 hours and at a temperature range of from -78° C. to room temperature. A temperature range of -78° C. to -40° C. and a reaction time of 15 minutes to 1 hour are preferred. The B-(2-(trisubstitutedsilyl)ethynyl)-9-boracyclo[3.3.1]nonane of formula (I) is isolated as a tetrahydrofuran complex by evaporation of the volatiles. It may be purified by crystallization from a suitable inert organic solvent such as pentane, hexane and the like. Starting materials for use in Scheme A are readily available to one of ordinary skill in the art.

1. waitranging from 5 minutes to 48 hours at a temperature range of from -78° C. to room temperature
2. customA temperature range of -78° C. to -40° C.
3. customa reaction time of 1.5 hours to 5 hours
4. customthus formed
5. stirringThe reactants are typically stirred together under an inert atmosphere for a period of time
6. waitranging from 5 minutes to 24 hours and at a temperature range of from -78° C. to room temperature
7. customA temperature range of -78° C. to -40° C.
8. customa reaction time of 15 minutes to 1 hour

ORD-Eintrag

ord-0f7509ed58e74952bba5c0f4c94f3faf

Quelldatensatz

uspto-grants-1992_10

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05157167