HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 18348749, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methylhydroxylamine | HCID 11647 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 69926500 | HCID 69926500 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 18348749 | HCID 18348749 | 79.4% |
Reaction Steps
A solution of 1.7 ml of oxalyl chloride in 15 ml of dichloromethane is added dropwise at 0° C. to a mixture of 4.8 g (15 mmol) of the compound of Example 8, 90 ml of dichloromethane and 1 ml of dimethylformamide. The solution obtained is stirred for 40 min and then added dropwise to a solution of 5.0 g of N-methylhydroxylamine in 15 ml of triethylamine, 10 ml of water and 60 ml of tetrahydrofuran. After stirring for 30 min, the mixture is treated with 20 ml of water and extracted with dichloromethane, the extract is dried and concentrated, and the residue is purified on silica gel (eluent trichloroethane/methanol 95:5). 3.4 g of title compound (78% of theory) are isolated, which after trituration with ether melt at 135-136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06326378B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-bbea42a4397f4abab1f84cdeeda27d3f |
| Source note | uspto-grants-2001_12 |