Sodium Hydroxide → 2,2-Dinitropropyl methyl ether

HRID 1165576Notes

Reaction equation

HRID 1165576 reaction equation
[OH-].[Na+].[CH3:3][O:4][CH2:5][CH:6]([N+:8]([O-:10])=[O:9])[CH3:7].[N:11]([O-:13])=[O:12].[Na+].S(OOS([O-])(=O)=O)([O-])(=O)=O.[Na+].[Na+]>O.[Fe-3](C#N)(C#N)(C#N)(C#N)(C#N)C#N.[K+].[K+].[K+].C(Cl)Cl>[CH3:3][O:4][CH2:5][C:6]([N+:11]([O-:13])=[O:12])([N+:8]([O-:10])=[O:9])[CH3:7]

Participants

8

Procedure

A solution of 1.0 g (25 mmoles) of sodium hydroxide in 10 mL of water was treated with 2.0 g (16.8 mmoles) of 2-nitropropyl methyl ether. After 10 minutes, 10 mL of methylene chloride was added, followed by a solution of 5.0 g (72 mmoles) of sodium nitrite in 10 mL of water. Next, a solution of 1.0 g (3 mmoles) of potassium ferricyanide in 5 mL of water was added, followed by 4.4 g (18 mmoles) of solid sodium persulfate. A cold water bath was used to moderate exothermic reaction. After 30 minutes, the reaction mixture was extracted with two 15 mL portions of methylene chloride. The combined extracts were washed with brine and dried over anhydrous magnesium sulfate. The solution was distilled in a short-path distillation apparatus to give 2.43 g (88% yield) of 2,2-dinitropropyl methyl ether, a colorless liquid, b.p. 100° (16 mm). 'H NMR (CDCl3): & 2.18 (s. 3H, --CH3), 3.35 (s, 3H, --OCH3), 4.15 (s, 2H, --CH2O).

Workup

  1. customA cold water bath was used
  2. customreaction
  3. waitAfter 30 minutes
  4. extractionthe reaction mixture was extracted with two 15 mL portions of methylene chloride
  5. washThe combined extracts were washed with brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationThe solution was distilled in a short-path distillation apparatus

Sources & evidence

ORD record
ord-b6adaca3f1c9454cb61cb1ef863f22bd
Source dataset
uspto-grants-1990_03
Patent number
US04910322

Reaction notes

Loading…