5-Aminovaleric acid → HCID 19808302, compound
Reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][C:6]([OH:8])=[O:7].CN(C)C(=N)N(C)C.[C:17]([O:21][C:22](N=[N+]=[N-])=[O:23])([CH3:20])([CH3:19])[CH3:18]>CN(C)C=O>[C:17]([O:21][C:22]([CH:5]([CH2:4][CH2:3][CH2:2][NH2:1])[C:6]([OH:8])=[O:7])=[O:23])([CH3:20])([CH3:19])[CH3:18]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
5-Amino pentanoic acid (0.585 g, 5 m mol) was stirred for two days in dimethylformamide (5 ml) containing tetramethylguanidine (1.14 g, 10 m mol) and tert.butoxycarbonylazide (1.1 g, 7.5 m mol). The solution was evaporated and the residue partitioned between ethyl acetate (20 ml) and 10% citric acid solution (20 ml). The organic layer was washed with 10% citric acid (2×15 ml), water (3×15 ml) and brine 1×15 ml). Each aqueous wash was back extracted with ethyl acetate (20 ml). The combined organic layers were dried over anhydrous magnesium sulphate and evaporated to give an oil which slowly crystallised. Recrystallisation from diisopropyl ether/petrol gave 0.745 g (70% yield), mp. 47.5°-48.5° C., Rf silica gel 0.40 (benzene:dioxan:acetic acid 95:75:4).
Workup
- customThe solution was evaporated
- customthe residue partitioned between ethyl acetate (20 ml) and 10% citric acid solution (20 ml)
- washThe organic layer was washed with 10% citric acid (2×15 ml), water (3×15 ml) and brine 1×15 ml)
- washEach aqueous wash
- extractionwas back extracted with ethyl acetate (20 ml)
- dry with materialThe combined organic layers were dried over anhydrous magnesium sulphate
- customevaporated
- customto give an oil which
- customslowly crystallised
- customRecrystallisation from diisopropyl ether/petrol
- customgave 0.745 g (70% yield), mp. 47.5°-48.5° C., Rf silica gel 0.40 (benzene:dioxan:acetic acid 95:75:4)
Sources & evidence
- ORD record
- ord-d2873f96791e4c92bdbf0021b8b14725
- Source dataset
- uspto-grants-1981_12
- Patent number
- US04304715
Reaction notes
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