HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → N-(2-tert-butyl-5-nitrophenyl)-2-(dimethylamino)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-bromo-N-(2-tert-butyl-5-nitrophenyl)acetamide | HCID 21961385 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-tert-butyl-5-nitrophenyl)-2-(dimethylamino)acetamide | HCID 21961377 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
2-Bromo-N-(2-tert-butyl-5-nitro-phenyl)-acetamide (Step B, 80 g, 253 mmol) and K2CO3 (70 g, 506 mmol) were combined in a 3 L 3-neck round bottom flask fitted with a mechanical stirrer, N2(g) inlet, and pressure equalizing addition funnel. THF (1.75 L) was added and the mixture cooled to 0° C. under N2(g). N,N-Dimethylamine (400 mL of a 2 M solution in THF, 800 mmol) was added to the mixture through the pressure equalizing addition funnel over 30 min. The mixture was gradually warmed to RT with stirring overnight. The reaction was quenched by filtering under vacuum and concentrating the filtrate under reduced pressure. The recovered material was eluted through a 36×7 cm column of silica gel with 50% EtOAc:Hexanes giving a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531553B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-338acbf132884d52a85c9a8c8ad80720 |
| Source note | uspto-grants-2009_05 |