Sodium Hydroxide → 2-Pyrimidineacetic Acid
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[N:3][C:2]=1[CH2:7][C:8]([O:10]CC)=[O:9].[OH-].[Na+]>C(O)C>[N:1]1[CH:6]=[CH:5][CH:4]=[N:3][C:2]=1[CH2:7][C:8]([OH:10])=[O:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of ethyl 2-(pyrimidin-2-yl)acetate (Example 31b, 410 mg. 2.47 mmol) in ethanol (5 mL) was added 2N NaOH (2 mL) at room temperature under nitrogen. The reaction mixture was stirred at room temperature under nitrogen for 72 hours, then concentrated under reduced pressure. The residue was triturated with ethanol and concentrated under reduced pressure to give the title compound, which was carried onto the next step without further purification. MS139 (MH+).
Workup
- concentrationconcentrated under reduced pressure
- customThe residue was triturated with ethanol
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-e3c2a0e7068844a2882eae0764e81ff0
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09138013B2
Reaction notes
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