Hydrochloric Acid → 2-Methyl-3-(pyridin-4-YL)propanoic acid
Reaction equation
Cl.[CH3:2][C:3]([CH2:14][C:15]1[CH:20]=[CH:19][N:18]=[CH:17][CH:16]=1)(C(OCC)=O)[C:4]([O:6]CC)=[O:5]>>[CH3:2][CH:3]([CH2:14][C:15]1[CH:20]=[CH:19][N:18]=[CH:17][CH:16]=1)[C:4]([OH:6])=[O:5]Participants
3
Procedure
Next, 6 N hydrochloric acid (96.8 ml, 581 mmol) was added to diethyl 2-methyl-2-(4-pyridylmethyl)malonate (17.2 g, 64.6 mmol), and the mixture was refluxed overnight. The reaction mixture was allowed to stand, then washed with hexane (100 ml) to remove sodium hydride oil contained in diethyl 2-methyl-2-(4-pyridylmethyl)malonate, and concentrated under reduced pressure. The resulting crystals were filtered off with ethyl acetate to give 10.7 g (82%) of 2-methyl-3-(4-pyridyl)propionic acid as pale pink crystals.
Workup
- temperaturethe mixture was refluxed overnight
- washwashed with hexane (100 ml)
- customto remove sodium hydride oil
- concentrationconcentrated under reduced pressure
- filtrationThe resulting crystals were filtered off with ethyl acetate
Sources & evidence
- ORD record
- ord-109194495d6746628c4db1843b6b45a0
- Source dataset
- uspto-grants-2008_03
- Patent number
- US07345064B2
Reaction notes
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