Dimethyl Sulfoxide → 2-Methyl-5-(oxiran-2-yl)pyridine
Reaction equation
CS(C)=O.[H-].[Na+].[I-].[CH3:8][S+](C)C.[CH3:12][C:13]1[CH:20]=[CH:19][C:16]([CH:17]=[O:18])=[CH:15][N:14]=1>C1COCC1>[CH3:12][C:13]1[CH:20]=[CH:19][C:16]([CH:17]2[CH2:8][O:18]2)=[CH:15][N:14]=1Participants
Conditions
- Temperature
- 65 °C
Procedure
The title compound was prepared by following general procedure 3. DMSO (4 mL) was added to NaH 60% dispersion in oil (0.314 g, 7.8 mmol, 1.3 equiv.) and heated to 65° C. for 1 h. THF (10 mL) was added at the same temperature and heated for another 10 min. After 10 min., the reaction mixture was cooled to 0° C. Trimethylsulfonium iodide (1.2 g, 5.9 mmol, 1 equiv.) was added and stirred for 10 min. and then a solution of 6-methylnicotinaldehyde (0.720 g, 5.9 mmol, 1 equiv.) in THF was added dropwise. After complete addition, the reaction mixture was stirred at RT for 2 h, the product was detected by LCMS. The reaction mixture was poured into ice water and the product was extracted in diethyl ether (4×50 mL), dried over Na2SO4 and concentrated at 25° C. to get the crude product 2-methyl-5-(oxiran-2-yl)pyridine (1.1 g crude).
Workup
- customThe title compound was prepared
- temperatureheated for another 10 min
- temperaturethe reaction mixture was cooled to 0° C
- additionAfter complete addition
- stirringthe reaction mixture was stirred at RT for 2 h
- extractionthe product was extracted in diethyl ether (4×50 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated at 25° C.
Sources & evidence
- ORD record
- ord-6356967570b44bd1a245acf526f6d616
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09409910B2
Reaction notes
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