Hydrochloric Acid → 2-Benzylacrylic Acid

HRID 1005302

Reaction equation

HRID 1005302 reaction equation
[CH2:1]([CH:8]([C:12](O)=O)[C:9]([OH:11])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(NCC)C.C=O.Cl>O>[CH2:1]([C:8](=[CH2:12])[C:9]([OH:11])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

6

Procedure

To a cooled (0° C.) mixture of benzyl malonic acid (3.37 g, 17.4 mmol) and diethylamine (1.34 g, 18.3 mmol) in water (10 ml) was added formaldehyde (37% solution in water, 2.1 g, 26.1 mmol) with stirring. The reaction was allowed to warm to room temperature and after 2 hours heated to reflux. After 16 hours, the reaction mixture was cooled to room temperature, then made acidic with hydrochloric acid. The mixture was extracted twice with ethyl acetate. The ethyl acetate layers were combined and dried over sodium sulfate, then the solvent was removed under reduced pressure. The resulting residue was purified by column chromatography to yield 2.2 g (78%) of white solid. 1H NMR (CDCl3): δ 3.7 (s, 2H), 5.6 (s, 1H) , 6.4 (s, 1H) , 7.1-7.4 (m, 5H)

Workup

  1. temperatureTo a cooled
  2. temperatureheated to reflux
  3. temperaturethe reaction mixture was cooled to room temperature
  4. extractionThe mixture was extracted twice with ethyl acetate
  5. dry with materialdried over sodium sulfate
  6. customthe solvent was removed under reduced pressure
  7. customThe resulting residue was purified by column chromatography

Sources & evidence

ORD record
ord-ff9c21a164d4487c82f295ce909f0292
Source dataset
uspto-grants-2000_04
Patent number
US06054444

Linked notes

Loading…