Methanol → HCID 66608971, compound
Reaction equation
[F:1][C:2]([F:15])([C:8]1[N:13]=[CH:12][C:11]([F:14])=[CH:10][N:9]=1)[C:3]([O:5]CC)=[O:4].CO.[OH-].[Na+:19]>C1COCC1>[F:15][C:2]([F:1])([C:8]1[N:13]=[CH:12][C:11]([F:14])=[CH:10][N:9]=1)[C:3]([O-:5])=[O:4].[Na+:19]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To ethyl 2,2-difluoro-2-(5-fluoropyrimidin-2-yl)acetate (470 mg, 2.13 mmol) were added MeOH (4 mL), THF (4 mL) and 1.2; N NaOH (2 mL, 2.4 mmol). The solution was stirred at rt for 30 min and then concentrated to dryness to afford sodium 2,2-difluoro-2-(5-fluoropyrimidin-2-yl)acetate (430 mg, 94%). 1H NMR (300 MHz, DMSO-d6) δ 8.94 (s, 2H).
Workup
- concentrationconcentrated to dryness
Sources & evidence
- ORD record
- ord-fe72608c006d4f10b8ae2667bff435b0
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08633207B2
Reaction notes
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