Synlett 2019; 30(01): 114-118
DOI: 10.1055/s-0037-1611362
letter
© Georg Thieme Verlag Stuttgart · New York

DDQ-Mediated Cross-Dehydrogenative-Coupling Reaction of Secondary Amines with Dialkyl Phosphonates

Ming-Xing Cheng*
College of Pharmacy, Henan University of Chinese Medicine, No. 156 Jinshui East Road, Zhengzhou 450046, P. R. of China   eMail: chengmx2018@hactcm.edu.cn
,
Jing-Wei Lei
,
Cai-Xia Xie
› Institutsangaben
Financial support from the Project of Science and Technology of Henan Province (No. 162102310448).
Weitere Informationen

Publikationsverlauf

Received: 29. September 2018

Accepted after revision: 09. November 2018

Publikationsdatum:
30. November 2018 (online)


Abstract

This work reports a DDQ-mediated cross-dehydrogenative-coupling reaction of secondary amines with dialkyl phosphonates under mild conditions. This reaction proceeds efficiently without involving visible light or transition-metal catalysis. This new approach provides efficient access to biologically important α-aminophosphonates.

Supporting Information

 
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  • 12 α-Aminophosphonates 3; General Procedure A Schlenk tube charged with secondary amine 1 (0.2 mmol) and DDQ (0.24 mmol, 1.2 equiv) was purged three times with argon. Anhyd toluene (2.0 mL) and phosphite 2 (0.36 mmol, 1.8 equiv) were added, and the mixture was stirred at 80 °C under Ar for 48 h. When the reaction was complete (TLC), the mixture was washed with sat. aq Na2CO3, concentrated, and purified by column chromatography (silica gel).
  • 13 Diethyl {(2E)-1-[(4-Bromophenyl)amino]-3-phenylprop-2-en-1-yl}phosphonate (3a) Viscous oil; yield: 78 mg (92%). 1H NMR (400 MHz, CDCl3): δ = 7.46–7.16 (m, 7 H), 6.67 (dd, J = 15.9, 4.8 Hz, 1 H), 6.62–6.50 (m, 2 H), 6.23 (dt, J = 16.0, 5.4 Hz, 1 H), 4.41 (dd, J = 19.4, 6.6 Hz, 2 H), 4.29–4.06 (m, 4 H), 1.30 (td, J = 7.1, 4.6 Hz, 6 H). 13C NMR (101 MHz, CDCl3): δ = 145.48 (d, J = 12.5 Hz), 136.00 (d, J = 3.2 Hz), 133.11 (d, J = 12.3 Hz), 131.93, 128.53, 127.93, 126.51 (d, J = 1.8 Hz), 122.83 (d, J = 4.6 Hz), 115.36 (d, J = 8.5 Hz), 110.15, 63.44 (d, J = 7.1 Hz), 63.08 (d, J = 7.2 Hz), 54.71, 53.18, 16.43 (t, J = 5.2 Hz). 31P NMR (162 MHz, CDCl3): δ = 21.92. MS (ESI): m/z = 424.1 [M + H]+.