Hydrochloric Acid → N,N'-Dimethoxy-N,N'-dimethyloxamide
Reaction equation
[CH3:1][NH:2][O:3][CH3:4].Cl.[C:6](Cl)(=[O:10])[C:7](Cl)=[O:8]>C(Cl)Cl.N1C=CC=CC=1>[CH3:1][N:2]([O:3][CH3:4])[C:7]([C:6]([N:2]([CH3:1])[O:3][CH3:4])=[O:10])=[O:8]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 48.0 g (0.49 mol) of N,O-dimethylhydroxylamine.HCl in 250 mL of 3:2 v/v CH2Cl2/pyridine was cooled to −78° C. and was treated with 17.4 mL (0.2 mol) of oxalyl chloride maintaining the internal temperature at less than −70° C. The resulting mixture was allowed to warm to rt and stirred for 20 h. The reaction was quenched with 250 mL of sat'd NaCl and the quenched mixture was extracted with 3×400 mL of CH2Cl2. The extracts were combined, dried over MgSO4 and concentrated. Recrystallization from 250 mL of MTBE afforded 24.28 g (69%) of the title compound: 1H NMR (500 MHz) δ 3.25 (s, 6H), 3.75 (s, 6H).
Workup
- customThe reaction was quenched with 250 mL of sat'd NaCl
- extractionthe quenched mixture was extracted with 3×400 mL of CH2Cl2
- dry with materialdried over MgSO4
- concentrationconcentrated
- customRecrystallization from 250 mL of MTBE
Sources & evidence
- ORD record
- ord-7e2d8544824540c5b4274ea3eed35829
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06498161B1
Reaction notes
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