HCID 57317184, compound → (2S,8S)-2,8-diaminononanedioic acid
Reaction equation
[NH2:1][C@@H:2]([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C@H:12]([NH2:17])[C:13]([O:15]C)=[O:14])[C:3]([O:5]C)=[O:4]>Cl>[NH2:1][C@@H:2]([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C@H:12]([NH2:17])[C:13]([OH:15])=[O:14])[C:3]([OH:5])=[O:4]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The ester from step (b) was heated under reflux in 6M HCl (7.2 ml) for 2 hours under N2. The volatile compounds were evaporated. The residue was dissolved in water (5 ml), ethanol was added (20 ml) and slow addition of ether led to a white, crystalline precipitate. This mixture was kept for 12 hours in the refrigerator, filtered, washed with ether and dried under vacuum.
Workup
- customThe volatile compounds were evaporated
- dissolutionThe residue was dissolved in water (5 ml)
- additionethanol was added
- addition(20 ml) and slow addition of ether
- filtrationfiltered
- washwashed with ether
- customdried under vacuum
Sources & evidence
- ORD record
- ord-03f79fba81054aef8cee0e16a51553e1
- Source dataset
- uspto-grants-1997_03
- Patent number
- US05610141
Reaction notes
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