HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Diisopropyl-6-methyl-1,2,3,4-tetrahydroquinoxaline → 7-Bromo-1,4-diisopropyl-6-methyl-1,2,3,4-tetrahydroquinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Diisopropyl-6-methyl-1,2,3,4-tetrahydroquinoxaline | HCID 22041393 | — |
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Bromo-1,4-diisopropyl-6-methyl-1,2,3,4-tetrahydroquinoxaline | HCID 22268301 | 70% |
Reaction Steps
A mixture of 1,4-diisopropyl-6-methyl-1,2,3,4-tetrahydroquinoxaline (516 mg, 2.22 mmol) and tetrabutylammonium tribromide (1.18 g, 2.45 mmol) in anhydrous dichloromethane (20 mL) was stirred at room temperature for 4 hours. The solution was washed successively with a saturated aqueous solution of NaHCO3 (150 mL), water (150 mL), a saturated aqueous solution of NaCl (150 mL), dried over MgSO4 and filtered. Removal of the solvent under reduced pressure gave a solid which was purified by column chromatography, using a Biotage 40S cartridge, eluting with 5% ethyl acetate/95% hexane, to give 7-bromo-1,4-diisopropyl-6-methyl-1,2,3,4-tetrahydroquinoxaline as a white solid (480 mg, 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06515003B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-51204edcdd8a42bb8d58b81055812505 |
| Source note | uspto-grants-2003_02 |