HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N,N'-Dimethoxy-N,N'-dimethyloxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N,O-Dimethylhydroxylamine | HCID 14232 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Solvent | Pyridine methylene chloride | HCID 21875418 | — |
| Product | N,N'-Dimethoxy-N,N'-dimethyloxamide | HCID 3287678 | 69% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06498161B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-7e2d8544824540c5b4274ea3eed35829 |
| Source note | uspto-grants-2002_12 |