REACTIVITY OF THE ACIDS OF TRIVALENT PHOSPHORUS AND THEIR DERIVATIVES. PART I. REDUCTIVE DEBROMINATION IN THE REACTIONS OF THE >P[sbnd]O⁻ IONS WITH 2-BROMOESTERS

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• Dimethyl 2,2-diphenylcyclopropanephosphonate: mp. 60–62°C; IR (KBr): v = 1260 (P[sbnd]O); 1050 (P[sbnd]O[sbnd]C) cm−1; 1H NMR, 200 MHz, (CDCl3) δ = 1.59 (ddd, J PH-10.62 Hz, J HH = 9.54 Hz, JHH = 4.17 Hz, 1H, CH); 1.85 (ddd, J PH = 2.60 Hz, J HH = 9.54 Hz, JHH = 6.72 Hz, 1H, CH); 2.05 (ddd, J PH = 19.17 Hz, J HH. = 6.72 Hz, J HH = 4.17 Hz, 1H, H[sbnd]C[sbnd]P); 3.24 (d, J PH = 10.78 Hz, 3H, OCH3); 3.59 (d, J PH., = 10.94 Hz, 3H, OCH3); 7.10–7.55 (m, 10H, C6H5). 31P NMR, 200 MHz (CDC13) δ = 29.07. MS exact mass calcd. for C17H19O3P: 302.1072; found: 302.1070
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