反应详情

温度

-78 °C

A cooled (−78° C.) solution of N,N-diisopropylamine (1.3 mL, 9.092 mmol, dried over calcium hydride) in anhydrous tetrahydrofuran (10 mL) was treated with a solution of n-butyllithium in hexanes (3.4 mL, 8.524 mmol, 2.5 M). After stirring at −78° C. for 30 minutes, the mixture was treated with a solution of morpholine-2,4-dicarboxylic acid 4-tert-butyl ester 2-methyl ester (1.394 g, 5.683 mmol) in anhydrous tetrahydrofuran (10 mL). After stirring at −78° C. for 20 minutes, the mixture was treated with acetaldehyde (0.96 mL, 17.05 mmol). After stirring at room temperature for 1 h, the reaction was quenched at 0° C. with hydrochloric acid (1 M, 40 mL). The aqueous layer was extracted with dichloromethane (2×). The organics were combined, filtered through a phase separator and the volatiles were removed in vacuo. The residue was purified by silica gel chromatography using a 50 g Isolute cartridge eluted with a continuous gradient of iso-hexanes/ethyl acetate 1:0 to 3:2 to afford the title compound (1.476 g, 90%) as a yellow oil and as a 2:1 mixture of diastereoisomers.

1. stirringAfter stirring at −78° C. for 20 minutes
2. stirringAfter stirring at room temperature for 1 h
3. customthe reaction was quenched at 0° C. with hydrochloric acid (1 M, 40 mL)
4. extractionThe aqueous layer was extracted with dichloromethane (2×)
5. filtrationfiltered through a phase separator
6. customthe volatiles were removed in vacuo
7. customThe residue was purified by silica gel chromatography
8. washeluted with a continuous gradient of iso-hexanes/ethyl acetate 1:0 to 3:2