Dimethyl Sulfoxide → 2-(N-allyloxycarbonyl-N-benzylamino)acetaldehyde
Reaction equation
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH2:11]([O:14][C:15]([N:17]([CH2:25][CH2:26][OH:27])[CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)=[O:16])[CH:12]=[CH2:13].C(N(CC)CC)C>ClCCl>[CH2:11]([O:14][C:15]([N:17]([CH2:25][CH:26]=[O:27])[CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)=[O:16])[CH:12]=[CH2:13]Participants
Procedure
To a solution of oxalyl chloride (13.8 ml) in dichloromethane (270 ml) was added dropwise a solution of dimethyl sulfoxide (19.7 ml) in dichloromethane (30 ml) below -60° C. under atmosphere of nitrogen. After stirring the mixture at the same condition for 30 minutes, a solution of 2-(N-allyloxycarbonyl-N-benzylamino)ethanol (32.6 g) in dichloromethane (30 ml) was added to the mixture below -60° C. with stirring. After 30 minutes, triethylamine (58 ml) was added to the mixture at the same condition. The mixture was stirred below -60° C. for 30 minutes and the reaction temperature was allowed to rise to ambient temperature. The mixture was washed with water (300 ml), 1N hydrochloric acid (300 ml×2), saturated aqueous sodium hydrogen carbonate (300 ml), and brine (300 ml) successively, dried over magnesium sulfate, and concentrated under reduced pressure to give 2-(N-allyloxycarbonyl-N-benzylamino)acetaldehyde (32.9 g) as a syrup.
Workup
- stirringwith stirring
- waitAfter 30 minutes
- stirringThe mixture was stirred below -60° C. for 30 minutes
- customto rise to ambient temperature
- washThe mixture was washed with water (300 ml), 1N hydrochloric acid (300 ml×2), saturated aqueous sodium hydrogen carbonate (300 ml), and brine (300 ml) successively
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-e836e8f2e5a14cef9123aa482181c032
- Source dataset
- uspto-grants-1992_04
- Patent number
- US05102877
Reaction notes
Loading…