Nitromethane → Methyl 3-methyl-4-nitrobutanoate

HRID 1360158

Reaction equation

HRID 1360158 reaction equation
[CH3:1][O:2][C:3](=[O:7])/[CH:4]=[CH:5]/[CH3:6].CN(C)C(=N)N(C)C.[N+:16]([CH3:19])([O-:18])=[O:17]>C(OC(=O)CC(C)=O)C>[CH3:1][O:2][C:3](=[O:7])[CH2:4][CH:5]([CH3:6])[CH2:19][N+:16]([O-:18])=[O:17]

Participants

5

Procedure

3 g (29.9 mmol) of trans-2-butenoic acid methyl ester and 0.69 g (5.99 mmol) of tetramethylguanidine and 9.14 g (149 mmol) of nitromethane were mixed. The resulting mixture was stirred at room temperature for 24 days. 100 mL of ethylacetoacetate was added to the solution and the reaction solution was washed with water, then an organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, then the residue was purified by column chromatography to give 5.7 g (23.6 mmol) of the title compound in a yield of 100%.

Workup

  1. washthe reaction solution was washed with water
  2. dry with materialan organic layer was dried over anhydrous magnesium sulfate
  3. distillationThe solvent was distilled off under reduced pressure
  4. customthe residue was purified by column chromatography

Sources & evidence

ORD record
ord-13469d9491184703a32c02a51d91c222
Source dataset
uspto-grants-2011_02
Patent number
US07879848B2

Linked notes

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