Diethyl Oxalate → Ethyl 4-(morpholin-4-yl)-2,4-dioxobutanoate

10.2 g of diisopropylamine (0.1 mol) was placed in 100 ml dry THF under nitrogen and cooled in a freezing mixture. 40 ml n-butyllithium in hexane (2.5 M, 0.1 mol) was slowly added dropwise. When the addition was completed the mixture was allowed to stir for 60 minutes and then acetylmorpholine 12.9 g (0.1 mol) was added dropwise. The reaction mixture was stirred for 20 min in the freezing mixture. In a second flask, 43.7 g of diethyl oxalate (0.3 mol) in 50 ml of dry THF was cooled in a freezing mixture and the cooled reaction mixture was cannulated with stirring in small portions to it. It was left overnight under stirring to warm to room temperature. The THF was removed on a rotary evaporator and the residue was taken up in 80 ml half concentrated hydrochloric acid. The aqueous phase was extracted five times with 150 ml ethyl acetate, and the combined organic phases were dried over sodium sulfate and concentrated on a rotary evaporator to dryness. The excess diethyl oxalate was removed by distillation (2-3 mbar, 80° C.). 5.0 g of product were obtained in the form of white crystals with a melting point of 60° C. after crystallization from PE (petrol ether).

1. temperaturecooled in a freezing mixture
2. additionWhen the addition
3. stirringThe reaction mixture was stirred for 20 min in the freezing mixture
4. customthe cooled reaction mixture
5. stirringwith stirring in small portions to it
6. waitIt was left overnight
7. stirringunder stirring
8. customThe THF was removed on a rotary evaporator
9. extractionThe aqueous phase was extracted five times with 150 ml ethyl acetate
10. dry with materialthe combined organic phases were dried over sodium sulfate
11. concentrationconcentrated on a rotary evaporator to dryness
12. customThe excess diethyl oxalate was removed by distillation (2-3 mbar, 80° C.)

ORDレコード

ord-f6264c969e8148aa8accdaf409e1c54c

出典データセット

uspto-grants-2016_07

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09394324B2