4-methyl-1-phenylmethoxypyrrolidine-2,3-dione

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 1-Benzyloxy-4-methylpyrrolidin-2,3-dione (7.8 g, 35.6 mmol) and R-(+)-.varies.-methylbenzylamine (8 ml, 7.5 g, 62 mmol) were stirred in methanol (250 ml) at 55° C. for 14 h then refluxed for 4 h. The mixture was then cooled, evaporated and purified by flash chromatography, eluting with hexanes: ethyl acetate (4:1 v/v) to give (R)-1-benzyloxy-4-methyl-2-oxo-3-(1-phenylethylamino)-2,5-dihydropyrrole (8.95 g, 78%) as a slightly yellow oil. 1H NMR (360 MHz, CDCl3) δ7.2-7.5 (10 H, m, Ph's), 5.00 (2 H, s, OCH2), 4.64 (1 H, q, J=6.8 Hz, NCH), 4.1 (1 H, br s, NH), 3.50 (1H, d, J=16.2 Hz, NCHAHB), 3.43 (1 H, d, J=16.2 Hz, NCHAHB), 1.60 (3 H, s, CH3CCH2), 1.45 (3 H, d, J=6.8 Hz, CH3CHPh), m/z (CI, NH3) 323 (M+ +H). then refluxed for 4 h The mixture was then cooled evaporated purified by flash chromatography eluting with hexanes: ethyl acetate (4:1 v/v)

Conditions: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Trifluoroacetic anhydride (30 ml, 44 g, 212 mmol) in dry dichlcromethane (100 ml) was added dropwise over 15 min to a stirred solution of dimethylsulphoxide (16 ml, 17.6 g, 259 mmol) in dry dichloromethane (500 ml) at -78° C. under nitrogen. After a further 10 min 1-benzyloxy-3-hydroxy-4-methylpyrrolidin-2-one (10 g, 45 mmol) in dichloromethane (80 ml) was added via cannula to the cloudy solution. After 30 min diisopropylethylamine (56 ml, 42 g, 330 mmol) was added dropwise over 5 min, and the reaction stirred for a further 35 min at -78° C. before being quenched at that temperature by the addition of methanol (20 ml). The mixture was then warmed to 0° C., washed with water (300 ml), and the water back extracted twice with dichloromethane. The combined organic layers were washed with brine, the brine extracted with dichloromethane, and the combined dichloromethane layers dried (Mg2SO4). After evaporation the product was purified by flash chromatography, eluting with dichloromethane: methanol (98:2 v/v) to give 1-benzyloxy-4-methylpyrrolidin-2,3-dione (7.8 g, 78%) as a white solid. In CDCl3 solution the ketone exists in its enol tautomeric form. 1H NMR (360 MHz, CDCl3) δ7.3-7.5 (5 H, m, Ph), 5.01 (2 H, s, OCH2), 3.61 (2 H, q, J=0.9 Hz, NCH2), 1.81 (3 H, t, J=0.9 Hz, CH3), m/z (CI, isobutane) 220 (M+ +H). before being quenched at that temperature by the addition of methanol (20 ml) The mixture was then warmed to 0° C. washed with water (300 ml) the water back extracted twice with dichloromethane The combined organic layers were washed with brine the brine extracted with dichloromethane the combined dichloromethane layers dried (Mg2SO4) After evaporation the product was purified by flash chromatography eluting with dichloromethane: methanol (98:2 v/v)