Hydrazine hydrate (1:1) → 4-Tert-butyl-5-hydroxymethylpyrazol-3-one
Reaction equation
[C:1]([CH:5]1[C:9](O)=[CH:8][O:7][C:6]1=[O:11])([CH3:4])([CH3:3])[CH3:2].O.[NH2:13][NH2:14]>CCO>[C:1]([C:5]1[C:6](=[O:11])[N:13]=[N:14][C:9]=1[CH2:8][OH:7])([CH3:4])([CH3:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3-tert-Butyl-4-hydroxy-2-furanone (6.6 g, 42 mmol) was dissolved in EtOH (75 mL) with hydrazine hydrate (6.6 mL, 0.21 mol) and was heated at reflux for 16h. The solvent was evaporated and the residue azeotroped with xylene ( 3×50 mL) to afford the title compound (7.2 g, 100%) as a colourless solid. mp 169-172° C. 1H NMR (360 MHz, d6-DMSO) δ1.26 (9H, s), 4.41 (2H, d, J=5.2 Hz), 4.97-5.01 (1H, m), 9.30 (1H, br s), 11.05 (1H, br s). MS (ES+) 171 (M+1).
Workup
- temperaturewas heated
- temperatureat reflux for 16h
- customThe solvent was evaporated
- customthe residue azeotroped with xylene ( 3×50 mL)
Sources & evidence
- ORD record
- ord-fbf2da12e00044a4ad889c32a84ebbd7
- Source dataset
- uspto-grants-2002_03
- Patent number
- US06355638B1
Reaction notes
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