Nitromethane → 1-(Nitromethyl)cyclobutanol
Reaction equation
[N+:1]([CH3:4])([O-:3])=[O:2].[O-]CC.[Na+].[C:9]1(=[O:13])[CH2:12][CH2:11][CH2:10]1>C(O)C>[N+:1]([CH2:4][C:9]1([OH:13])[CH2:12][CH2:11][CH2:10]1)([O-:3])=[O:2]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Under a nitrogen atmosphere, nitromethane (116 mL, 2.14 mol) and sodium ethoxide (2.6 g of 96% pure material, 36 mmol) were sequentially added to a solution of cyclobutanone (50.0 g, 713 mmol) in ethanol (71 mL), and the resulting solution was stirred at room temperature for 4 days. Some of the ethanol was removed under reduced pressure, and water (100 mL) was added. The resulting mixture was extracted with ethyl acetate (3×150 mL). The combined extracts were washed sequentially with water (2×80 mL) and brine (40 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by vacuum distillation under high vacuum at 70° C. to provide 46.1 g of 1-(nitromethyl)cyclobutanol as an orange liquid.
Workup
- customSome of the ethanol was removed under reduced pressure, and water (100 mL)
- additionwas added
- extractionThe resulting mixture was extracted with ethyl acetate (3×150 mL)
- washThe combined extracts were washed sequentially with water (2×80 mL) and brine (40 mL)
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- distillationThe residue was purified by vacuum distillation under high vacuum at 70° C.
Sources & evidence
- ORD record
- ord-63e4e516ccc84e44bcaa713c2c730ba3
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07884207B2
Reaction notes
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