Ethylene Glycol → N-methyl-N-(1,3-dioxolan-2-ylmethyl)-alpha-chloroacetamide
Reaction equation
[CH3:1][N:2]([CH2:7][CH:8]([O:11][CH3:12])[O:9][CH3:10])[C:3](=[O:6])[CH2:4][Cl:5].C(O)CO.C1(C)C(S(O)(=O)=O)=CC=CC=1.C(=O)([O-])[O-].[Na+].[Na+]>CCOCC.CO>[CH3:1][N:2]([CH2:7][CH:8]1[O:11][CH2:12][CH2:10][O:9]1)[C:3](=[O:6])[CH2:4][Cl:5]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
N-Methyl-N-(2,2-dimethoxyethyl)-α-chloroacetamide (19.5 grams; 0.10 mole), ethylene glycol (6.82 grams; 0.11 mole) and 10 drops of a solution of toluene sulfonic acid (1 gram) in ether (100 ml) were charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and distillation head. The mixture was heated at 100° to 110° C. with stirring and the methanol removed as it was formed. After no more methanol was given off the reaction mixture was cooled to room temperature and was stirred with about 2 grams of sodium carbonate for a period of about 1 hour. After this time the reaction mixture was filtered and the filtrate was distilled under reduced pressure to yield the desired product N-methyl-N-(1,3-dioxolan-2-ylmethyl)-α-chloroacetamide having a boiling point of 119° to 124° C. at a pressure of 0.15 to 0.30 mm of Hg.
Workup
- customequipped with a mechanical stirrer
- distillationthermometer and distillation head
- temperatureThe mixture was heated at 100° to 110° C.
- customthe methanol removed as it
- customwas formed
- filtrationAfter this time the reaction mixture was filtered
- distillationthe filtrate was distilled under reduced pressure
Sources & evidence
- ORD record
- ord-03274e1e05134b8cb3fd790d10e26a49
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04113464
Reaction notes
Loading…