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tert-butyl (1R,2R)-2-aMinocyclopentylcarbaMate synthesis

2synthesis methods
245115-25-7 Synthesis
(1S,2R)-Boc-2-amino-1-cyclopentanecarboxylic acid

245115-25-7
80 suppliers
$40.00/100 mg

-

Yield:-

Steps:

Multi-step reaction with 4 steps
1.1: Et3N; ethyl chloroformate / tetrahydrofuran / 0.33 h / 0 °C
1.2: aq. NaN3 / tetrahydrofuran / 0.33 h / 0 °C
2.1: benzene / 0.5 h / Heating
3.1: CuCl / dimethylformamide / 0.75 h / 20 °C
4.1: H2 / Pd/C / methanol / 12 h / 2844.31 Torr

References:

Pokorski, Jonathan K.;Witschi, Mark A.;Purnell, Bethany L.;Appella, Daniel H. [Journal of the American Chemical Society,2004,vol. 126,# 46,p. 15067 - 15073]