Abstract
A simple, efficient, and general method has been developed for
the synthesis of α-aminophosphonic esters using TsCl as an
efficient catalyst. α-Aminophosphonic acids were obtained
in good to high yields (65-85%) and purity under
mild conditions by the reaction of diethyl phosphite with imines
in the presence of TsCl.
Key words
α-aminophosphonates - imines - alkyl
phosphite -
p -tosyl chloride - addition reaction
References and Notes
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TsCl (1 mmol, 0.18 g) was added to
a stirred mixture of diethyl phosphite (0.012 mol) in CH2 Cl2 (10
mL) at r.t. Imine (0.01 mol) was added to the reaction mixture and
the mixture was stirred for 2-4 h at r.t. H2 O
(50 mL) was added to the reaction mixture and the organic layer
was extracted with EtOAc (4 × 50 mL), dried with CaCl2 ,
and the solvent was evaporated to give the crude product. Chromatography on
silica gel with EtOAc-n -hexane
(1:9 → 5:5) and evaporation of the solvent under reduced
pressure gave the pure products in 65-85% yields.
All the products gave satisfactory spectral data in accordance with
the assigned structures and literature reports.
[¹²a ]
[¹6b ]
Diethyl[phenyl(phenylamino)methyl]phosphonate
(2a) : ¹ H NMR (250 MHz,
CDCl3 ): δ = 1.13 (t, J = 7.0
Hz, 3 H), 1.29 (t, J = 7.0 Hz,
3 H), 3.60-3.75 (m, 1 H), 3.85-4.01 (m, 1 H),
4.03-4.22 (m, 2 H), 4.76 (d, J
HP = 24.2
Hz, 1 H), 6.59 (d, J = 8.5 Hz,
2 H), 6.69 (t, J = 7.2 Hz, 1
H), 7.11 (t, J = 8.3 Hz, 2 H),
7.22-7.52 (m, 5 H). ³¹ P NMR
(101.2 MHz, CDCl3 , H3 PO4 ): δ = 23.31. ¹³ C
NMR (62.9 MHz, CDCl3 ): δ = 16.2 (d, J
PC = 6.3 Hz), 16.4
(d, J
PC = 6.3 Hz),
56.1 (d, J
PC = 150.3 Hz),
63.1, 63.2, 113.8, 118.3, 127.9 (d, J
PC = 5.7
Hz), 128.5 (d, J
PC = 2.5
Hz), 129.2, 136.0 (d, J
PC = 2.5
Hz), 146.3 (d, J
PC = 14.5
Hz).