Sodium Hydroxide → Glycine tert-butyl ester
Reaction equation
Cl.[C:2]([O:6][C:7](=[O:10])[CH2:8][NH2:9])([CH3:5])([CH3:4])[CH3:3].[OH-].[Na+]>>[C:2]([O:6][C:7](=[O:10])[CH2:8][NH2:9])([CH3:5])([CH3:4])[CH3:3]Participants
3
Procedure
Glycine t-butyl ester hydrochloride (2.51 g, 15 mmol) was treated with 10N aqueous sodium hydroxide (1.6 ml) and extracted with dichloromethane (50 ml). The dichloromethane solution was back washed with saturated aqueous sodium chloride (2×5 ml), dried over sodium sulfate, and concentrated in vacuo to yield the glycine t-butyl ester (1.38 g, 70% yield).
Workup
- extractionextracted with dichloromethane (50 ml)
- washThe dichloromethane solution was back washed with saturated aqueous sodium chloride (2×5 ml)
- dry with materialdried over sodium sulfate
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-92f444f82f3c4e59af9f7f196b2823da
- Source dataset
- uspto-grants-1997_03
- Patent number
- US05607691
Reaction notes
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