반응 #89704

반응 방정식

triethylamine

oxalyl chloride

1,2-dibenzyl 3-tert-butyl(2S,3S)-5-hydroxypiperidine-1,2,3-tricarboxylate

dimethyl sulfoxide

→

ketone

수율 100.0%

1,2-dibenzyl 3-tert-butyl(2S,3S)-5-oxopiperidine-1,2,3-tricarboxylate

수율 100.0%

용매

methylene chloride

methylene chloride

methylene chloride

반응 조건

후처리

1. 1
   기타To an oven-dried 5 mL conical vial equipped with a magnetic stir bar and under a nitrogen gas atmosphere
2. 2
   온도to gradually warm to ca. 0° C. over 1.5 h
3. 3
   온도The reaction mixture was cooled to 78° C.
4. 4
   workup.STIRRINGstirring
5. 5
   workup.WAITwas continued for 3 h
6. 6
   온도with gradual warming to ca. 0° C
7. 7
   기타The reaction was quenched by the dropwise addition of 5% citric acid (2 mL)
8. 8
   workup.ADDITIONdiluted with methylene chloride (15 mL)
9. 9
   세척The organic layer was washed with brine (2×5 mL)
10. 10
    건조dried (NaSO4)
11. 11
    농축concentrated in-vacuo

실험 절차

To an oven-dried 5 mL conical vial equipped with a magnetic stir bar and under a nitrogen gas atmosphere was placed oxalyl chloride (0.080 mL, 0.92 mmol) and methylene chloride (0.7 mL). The solution was cooled to 78° C. prior to the dropwise addition of dimethyl sulfoxide (0.080 mL, 1.13 mmol) in methylene chloride (0.3 mL). After stirring the solution for 45 min, a solution of 1,2-dibenzyl 3-tert-butyl(2S,3S)-5-hydroxypiperidine-1,2,3-tricarboxylate (266 mg, 0.567 mmol) in methylene chloride (1 mL) was added dropwise and the solution was allowed to gradually warm to ca. 0° C. over 1.5 h. The reaction mixture was cooled to 78° C. prior to the dropwise addition of triethylamine (0.240 mL, 1.72 mmol) and stirring was continued for 3 h with gradual warming to ca. 0° C. The reaction was quenched by the dropwise addition of 5% citric acid (2 mL) and diluted with methylene chloride (15 mL). The organic layer was washed with brine (2×5 mL), dried (NaSO4), and concentrated in-vacuo to afford 264 mg (100%) of the desired ketone as a sticky yellow oil. LCMS (ESI): 490 (M+Na+)

출처