Dimethyl Sulfoxide → 2-Methoxy-6-methyl-3-nitropyridine-4-carbaldehyde
반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[OH:11][CH2:12][C:13]1[CH:18]=[C:17]([CH3:19])[N:16]=[C:15]([O:20][CH3:21])[C:14]=1[N+:22]([O-:24])=[O:23].CCN(CC)CC>C(Cl)Cl>[CH:12]([C:13]1[CH:18]=[C:17]([CH3:19])[N:16]=[C:15]([O:20][CH3:21])[C:14]=1[N+:22]([O-:24])=[O:23])=[O:11]참가 물질
6
반응 조건
- 온도
- -70 °C
실험 절차
To a −70° C. solution of oxalyl chloride (2.0 mL, 22 mmol) in 50 mL of DCM was added 3.4 mL (44 mmol) of DMSO in 10 mL of DCM by dropping funnel. After 2 min, the reaction mixture was treated with 3.99 g (20 mmol) of the alcohol from step C in 20 mL of DCM. The solution was stirred for an additional 15 min at −70° C., treated with 14 mL (50 mmol) of Et3N and warmed to ambient temperature over 90 min. The reaction was quenched with 100 mL of water and the two phases were separated. The aqueous phase was extracted with 100 mL of DCM and the combined organic extracts were washed with 50 mL of brine and dried over MgSO4. The yellow solution was concentrated and chromatographed (2:3 EtOAc/Hexane) to afford the aldehyde as a yellow solid.
후처리
- temperaturewarmed to ambient temperature over 90 min
- customThe reaction was quenched with 100 mL of water
- customthe two phases were separated
- extractionThe aqueous phase was extracted with 100 mL of DCM
- washthe combined organic extracts were washed with 50 mL of brine
- dry with materialdried over MgSO4
- concentrationThe yellow solution was concentrated
- customchromatographed (2:3 EtOAc/Hexane)
출처 및 근거
- ORD 기록
- ord-ae5b1a02a1f148f8a657d64c063a76e1
- 출처 데이터셋
- uspto-grants-2003_08
- 특허 번호
- US06610692B1
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