Tricyclohexylphosphonium Tetrafluoroborate

Tricyclohexylphosphine tetrafluoroborate may be used in the following processes: As a ligand for preparing C-homoaporphine alkaloids via microwave-assisted direct-arylation; To synthesize poly-[9,9-bis(3-propylamide-2-methylpropyl sulfonic acid) fluorene]-co-(4,4'-diphenyl) (PFDBSO3H), which can be employed as a template and doping agent for enhancing the conductivity of poly(3,4-ethylenedioxythiophene) (PEDOT) films; To improve the reactivity of palladium-catalyzed Suzuki-Miyaura cross-coupling reaction between MIDA boronates and less activated alkenyl tosylates. Used with Ru(cod)Cl dimer to catalyze the dehydrogenative coupling of alcohols and amines to form amide bonds.

tricyclohexylphosphonium;tetrafluoroborate; tricyclohexylphosphanium;tetrafluoroborate

tricyclohexylphosphanium;tetrafluoroborate

[B-](F)(F)(F)F.C1CCC(CC1)[PH+](C2CCCCC2)C3CCCCC3

InChI=1S/C18H33P.BF4/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;2-1(3,4)5/h16-18H,1-15H2;/q;-1/p+1

MYSMMEUXKHJYKH-UHFFFAOYSA-O

164 °C (lit.)

Not applicable

97 %

7.49870

P260, P261, P264, P270, P271, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501

Danger