HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → 4-bromo-N-methoxy-N,2-dimethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 4-Bromo-2-methylbenzoic acid | HCID 99570 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-bromo-N-methoxy-N,2-dimethylbenzamide | HCID 18970485 | 91.6% |
Reaction Steps
To the solution of compound 4-bromo-2-methylbenzoic acid D-1 (50 g, 0.23 mol) in DCM (500 mL) was added EDCI (48 g, 0.25 mol), HOBt (34.1 g, 0.25 mol), NMM (50.5 g, 0.50 mol) and N,O-dimethylhydroxylamine hydrochloride (24.3 g, 0.25 mol). The reaction mixture was stirred at room temperature overnight, diluted with DCM, washed with H2O (300 mL), 1 N HCl (300 mL), and saturated sodium bicarbonate solution (300 mL), dried over sodium sulfate, and concentrated to give the desired product D-2 (55 g, yield 91.6%) as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642628B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-b8ce98ff65dd4b4d93cdb62d991571b3 |
| Source note | uspto-grants-2014_02 |