Hydrazine → 3-(trifluoromethyl)-1H-pyrazol-5-amine
Reaction equation
[NH2:1]/[C:2](/OCC)=[CH:3]\[C:4](=O)[C:5]([F:8])([F:7])[F:6].[NH2:13][NH2:14]>CCO>[F:6][C:5]([F:8])([F:7])[C:4]1[NH:14][N:13]=[C:2]([NH2:1])[CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
A mixture of (E)-4-amino-4-ethoxy-1,1,1-trifluorobut-3-en-2-one (5.00 g, 27 mmol) and hydrazine (1.05 g) in anhydrous EtOH (20 mL) was stirred at 80° C. in a sealed vial overnight. The reaction was quenched with water (50 mL), and extracted with EtOAc (100 ml, then 2×50 mL). The EtOAc layers were combined and sequentially washed with water (25 mL), brine (25 mL), dried over Na2SO4 and evaporated to give a light brown oily residue. The crude product was purified by silica chromatography (30-100% EtOAc in hexanes gradient) to give 5-(trifluoromethyl)-1H-pyrazol-3-amine as an off white solid; ESMS m/z 152.0 (M+H+).
Workup
- customThe reaction was quenched with water (50 mL)
- extractionextracted with EtOAc (100 ml
- washsequentially washed with water (25 mL), brine (25 mL)
- dry with materialdried over Na2SO4
- customevaporated
- customto give a light brown oily residue
- customThe crude product was purified by silica chromatography (30-100% EtOAc in hexanes gradient)
Sources & evidence
- ORD record
- ord-3a987e84a18b4d508bbce2aee4d78131
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08859574B2
Reaction notes
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