Reaction equation
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][C:6]([NH:8][NH2:9])=[O:7].[ClH:10].C(OCC)(=O)C>C(OCC)(=O)C>[ClH:10].[CH3:1][O:2][CH2:3][CH2:4][CH2:5][C:6]([NH:8][NH2:9])=[O:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N′-(4-Methoxybutyryl)hydrazine carboxylic acd tert-butyl ester (9.30 g) was dissolved in ethyl acetate (50 ml), followed by addition of 4 mol/liter hydrochloric acid/ethyl acetate solution (150 ml), and stirred at ambient temperature for 2 hours. After the reaction solution was concentrated under reduced pressure, the resulting residue was washed with n-hexane, to afford 4-methoxybutyric acid hydrazide hydrochloride salt as pale yellow solid (5.99 g, 89%). The physico-chemical values are as follows.
Workup
- concentrationAfter the reaction solution was concentrated under reduced pressure
- washthe resulting residue was washed with n-hexane
Sources & evidence
- ORD record
- ord-2f1fc4e63bcd49baab4faaaf5cb38cf8
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07084164B2
Linked notes
Loading…