HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 6-bromo-N-methoxy-N-methyl-2-Naphthalenecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 6-Bromo-2-naphthoyl chloride | HCID 21879606 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-bromo-N-methoxy-N-methyl-2-Naphthalenecarboxamide | HCID 59813225 | 100% |
Reaction Steps
N,O-Dimethylhydroxylamine Hydrochloride (41.3 g, 423 mmol, 1.5 equiv.) was dissolved in distilled water (200 mL) and potassium carbonate (117 g, 3.0 equiv.) was added portion wise (CO2 evolution). Water (300 mL) and dichloromethane (200 mL) was added and a solution of 6-bromo-2-naphthoyl chloride (76.1 g, 282 mmol, 1.00-equiv.) in dichloromethane (300 mL) was added portion wise to this mixture while stirring. The reaction mixture was stirred 1 hour. The organic layer was separated, dried over sodium sulphate, filtrated, concentrated and dried in vacuum overnight, yielding 6-bromo-N-methoxy-N-methyl-2-naphthamide (82.9 g, 100%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09427428B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-d428ed0efa5b42efae59e69b0b928478 |
| Source note | uspto-grants-2016_08 |