Reaktion #698979

Reaktionsgleichung

toluene

EtOAc

Spinosyn H

Diethyl chlorophosphite

→

(diethyl)phosphite

Spinosyn H

Lösungsmittel

pyridine

Reaktionsbedingungen

Aufarbeitung

1. 1
   WaschenThe solution was washed successively with brine (2×) and 5% aq. NaHCO3
2. 2
   TrocknenThe organic layer was dried over Na2SO4
3. 3
   Einengenconcentrated
4. 4
   SonstigeThe residue was separated over a flash SiO2 column (100 g/EtOAc)

Vorschrift

Compound Spinosyn H (351 mg, 0.489 mmol) was dissolved in dry pyridine (5 ml). DMAP (62 mg, 0.51 mmol) was added and stirring at RT under nitrogen was continued for 5 min. Diethyl chlorophosphite (157 mg, 0.145 ml, 1.0 mmol) was added. After 30 min. toluene (50 ml) and EtOAc (50 ml) were added. The solution was washed successively with brine (2×) and 5% aq. NaHCO3. The organic layer was dried over Na2SO4 and concentrated. The residue was separated over a flash SiO2 column (100 g/EtOAc) to give compound 2'R)-(diethyl)phosphite of Spinosyn H; 306 mg, 75% CI MS m/z 838 (M+1); 1H-NMR (CDCl3) δ 6.69 (1H, bs), 4.40 (1H, m), 3.83 (4H, 2× CH2, m), 1.18 (6H, 2× CH3, m); Elemental Analysis: for C44H72NO12P calc. C 63.06, H 8.66, N 1.67 found: C 62.94, H 8.88, N 1.71.

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