HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 6-Bromo-1-methyl-1,2,3,4-tetrahydroquinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 59418741 | HCID 59418741 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Bromo-1-methyl-1,2,3,4-tetrahydroquinoxaline | HCID 59418738 | 101.1% |
Reaction Steps
A solution of 4-bromo-N′-(2-chloroethyl)-N′-methylbenzene-1,2-diamine (25D) (0.611 g, 2.3 mmol) and K2CO3 (0.634 g, 4.6 mmol) in DMF (7 mL) was heated to 80° C. for 1 hour and then at 100° C. for 1.5 hours, cooled to rt, diluted with water and extracted with EtOAc. The organic phases were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to provide 0.528 g (100%) of the desired product 6-bromo-1-methyl-1,2,3,4-tetrahydroquinoxaline (25E): 1H NMR (300 MHz, CDCl3) δ 6.72 (1H, dd), 6.56 (1H, d), 6.38 (1H, d), 3.74 (1H, bs), 3.47 (2H, t), 3.22 (2H, t), 2.82 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067928B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-b81ebc6309324aab83d726e766fa2979 |
| Source note | uspto-grants-2015_06 |