Lithium Hydroxide → 4-Nitro-1H-pyrazole-1-propanoic acid
Reaction equation
[N+:1]([C:4]1[CH:5]=[N:6][NH:7][CH:8]=1)([O-:3])=[O:2].C[O:10][C:11](=[O:15])[CH2:12][CH2:13]Br.C(=O)([O-])[O-].[K+].[K+].[OH-].[Li+]>CN(C=O)C.CO>[N+:1]([C:4]1[CH:5]=[N:6][N:7]([CH2:13][CH2:12][C:11]([OH:15])=[O:10])[CH:8]=1)([O-:3])=[O:2]Participants
7
Conditions
- Temperature
- 50 °C
Procedure
4-Nitro-1H-pyrazole (0.50 g, 4.4 mmol) was dissolved in DMF (5 mL). After addition of methyl-3-bromopropionate (0.72 mL, 1.5 eq) and potassium carbonate (0.92 g, 1.5 eq), the reaction mixture was stirred at 50° C. for 3 h, then partitioned between water and DCM. The aqueous phase was extracted with DCM, the combined organic phases dried over sodium sulfate and evaporated. The residue was hydrolyzed at rt over 30 min with lithium hydroxide (3M, aqueous) (4.4 mL, 3 eq) in methanol (5 mL) and the reaction mixture evaporated to dryness to afford 3-(4-nitro-1H-pyrazol-1-yl)propanoic acid in a quantitative yield.
Workup
- custompartitioned between water and DCM
- extractionThe aqueous phase was extracted with DCM
- dry with materialthe combined organic phases dried over sodium sulfate
- customevaporated
- customthe reaction mixture evaporated to dryness
Sources & evidence
- ORD record
- ord-b88fef098df14fb59c6dacf5fc2a0e3c
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09040545B2
Reaction notes
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