2-Methyl-2-(4-nitrophenyl)-1,3-dioxolane → HCID 67491648, compound

HRID 2240644Notes

Reaction equation

HRID 2240644 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]1

Participants

3

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

  1. filtrationThen the catalyst is filtered off
  2. concentrationthe filtrate is concentrated by evaporation
  3. dissolutionThe residue is dissolved in cyclohexane
  4. filtrationfiltered
  5. customto remove insoluble matter
  6. 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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