Diethylamine → HCID 86678720, compound
Reaction equation
CC1C=CC(S(O[CH2:12][CH2:13][O:14][CH2:15][CH2:16][NH:17][C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])(=O)=O)=CC=1.[CH2:25]([NH:27][CH2:28][CH3:29])[CH3:26].[OH-].[Na+]>C1COCC1>[C:21]([O:20][C:18](=[O:19])[NH:17][CH2:16][CH2:15][O:14][CH2:13][CH2:12][N:27]([CH2:28][CH3:29])[CH2:25][CH3:26])([CH3:22])([CH3:23])[CH3:24]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 2-{2-[(tert-butoxycarbonyl)amino]ethoxy}ethyl 4-methylbenzenesulfonate (5.00 g) in THF (40 mL) was added diethylamine (14.5 mL). The reaction mixture was stirred at room temperature overnight, and 1N aqueous sodium hydroxide solution was added. The mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (3.77 g).
Workup
- extractionThe mixture was extracted with ethyl acetate
- dry with materialdried over anhydrous magnesium sulfate
- customthe solvent was evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-fff69b2bde6843199a3007f3f5a8728a
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08772277B2
Reaction notes
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