Methyl 3-oxo-3-phenylpropanoate → Methyl 3-amino-3-phenylprop-2-enoate

HRID 1367756Notes

Reaction equation

HRID 1367756 reaction equation
[C:1]([CH2:9][C:10]([O:12][CH3:13])=[O:11])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([O-])=O.[NH4+:17]>CO>[NH2:17][C:1]([C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[CH:9][C:10]([O:12][CH3:13])=[O:11]

Participants

4

Procedure

To a solution of 40.00 g (0.2245 mol) of methyl benzoylacetate in 400 ml of methanol, 70.30 g (1.115 mol) of ammonium formate was added and the mixture was refluxed for 18 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, and the solvent was distilled away under reduced pressure. To the residue, 200 ml of ethyl acetate and 150 ml of water were added, and the mixture was stirred at room temperature for 30 minutes. Then, the organic layer was separated, and the aqueous layer was extracted with 100 ml of ethyl acetate. The organic layer and the extract were combined, washed with water and a brine successively and dried with sodium sulfate. The solvent was removed under reduced pressure, and the residue was then distilled to give the objective methyl 3-amino-3-phenylacrylate (32.44 g, a colorless oil). The yield was 81.6%.

Workup

  1. temperaturethe mixture was refluxed for 18 hours
  2. customAfter completion of the reaction
  3. distillationthe solvent was distilled away under reduced pressure
  4. additionTo the residue, 200 ml of ethyl acetate and 150 ml of water were added
  5. customThen, the organic layer was separated
  6. extractionthe aqueous layer was extracted with 100 ml of ethyl acetate
  7. washwashed with water
  8. dry with materiala brine successively and dried with sodium sulfate
  9. customThe solvent was removed under reduced pressure
  10. distillationthe residue was then distilled

Sources & evidence

ORD record
ord-65ddd76a57bc4a1baa2e515dcbb9b2da
Source dataset
uspto-grants-2011_02
Patent number
US07893296B2

Reaction notes

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