2-Methyl-2-(4-nitrophenyl)-1,3-dioxolane → HCID 67491648, compound
Reaction equation
[CH3:1][C:2]1([C:7]2[CH:12]=[CH:11][C:10]([N+:13]([O-])=O)=[CH:9][CH:8]=2)[O:6][CH2:5][CH2:4][O:3]1>CO>[CH3:1][C:2]1([CH:7]2[CH2:12][CH2:11][CH:10]([NH2:13])[CH2:9][CH2:8]2)[O:3][CH2:4][CH2:5][O:6]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
8.37 g (40 mmol) of 2-methyl-2-(4-nitrophenyl)-[1,3]dioxolane is placed in 160 mL of methanol and hydrogenated with 1.00 g of Nishimura catalyst at ambient temperature under a pressure of 50 psi. Then the catalyst is filtered off and the filtrate is concentrated by evaporation. The residue is dissolved in cyclohexane, filtered to remove insoluble matter, and the filtrate is evaporated to dryness. Yield: 7.00 g (94%), cis/trans ratio 77:23; NMR: LG201616.
Workup
- filtrationThen the catalyst is filtered off
- concentrationthe filtrate is concentrated by evaporation
- dissolutionThe residue is dissolved in cyclohexane
- filtrationfiltered
- customto remove insoluble matter
- customthe filtrate is evaporated to dryness
Sources & evidence
- ORD record
- ord-9e059d561ab44fe0b75a6c7f65086ff4
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07723381B2
Reaction notes
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