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174293-30-2

Cyclohexanol, 2-(1-piperidinyl)-, (1S,2S)- synthesis

1synthesis methods
-

Yield:174293-30-2 96%

Reaction Conditions:

with ferrocenium(III) tetrafluoroborate in neat (no solvent) at 60; for 6 h;regioselective reaction;

Steps:

β-Amino Alcohols; General Procedure

General procedure: Catalyst Fe(Cp)2BF4 (5 mol%) was added to the cooled epoxide (2 mmol) at 0-5 °C and then amine (2.1 mmol) was added. The resulting mixture was stirred at 25 °C for the specified time (TLC monitoring). When the reaction was complete, the crude product was purified by column chromatography. For entry 9 in Table 1, CH2Cl2(0.5 mL) was used as solvent.

References:

Yadav, Geeta Devi;Chauhan, Manmohan Singh;Singh, Surendra [Synthesis,2014,vol. 46,# 5,p. 629 - 634]