HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-2-methylaniline → N2-(3-chloro-2-methylphenyl)-N-(4-methoxybenzyl)glycinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-2-methylaniline | HCID 6894 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-N-(4-methoxybenzyl)acetamide | HCID 46736691 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N2-(3-chloro-2-methylphenyl)-N-(4-methoxybenzyl)glycinamide | HCID 26417493 | 65.9% |
Reaction Steps
3.93 g of 3-chloro-2-methylaniline was dissolved in 10 mL of DMF, and 2.00 g of potassium carbonate was added thereto, followed by portionwise addition of 3.55 g of 2-bromo-N-(4-methoxybenzyl)acetamide over 1 hour. The mixture was stirred at room temperature overnight, and ice water was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with brine, and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=70:30 to 30:70) to obtain 2.89 g of N2-(3-chloro-2-methylphenyl)-N-(4-methoxybenzyl)glycinamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07973078B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-487d1c7550d14bbda2bcd20b348ee1ee |
| Source note | uspto-grants-2011_07 |