HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 6,7-Dichloro-2,3-dimethoxy-5-(1-hydroxyethyl)quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 6,7-Dichloro-2,3-dimethoxy-5-formylquinoxaline | HCID 10493492 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6,7-Dichloro-2,3-dimethoxy-5-(1-hydroxyethyl)quinoxaline | HCID 19068884 | 91.1% |
Reaction Steps
Methylmagnesium bromide (2.3 mL, 1M in di-n-butylether, 2.3 mmol) was added to a suspension of 6,7-dichloro-2,3-dimethoxy-5-formylquinoxaline (600 mg, 2.09 mmol) in dry tetrahydrofuran (30 mL) under nitrogen at room temperature. After 30 minutes, saturated ammonium chloride (20 mL) was added, and the product was extracted into ethyl acetate (2×30 mL). The combined extracts were dried (MgSO4) and concentrated under reduced pressure to give 6,7-dichloro-2,3-dimethoxy-5-(1-hydroxyethyl)quinoxaline (577 mg, 91%), as a creamy coloured solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05783572 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-967ebc73364e491b8612c8b206a237e6 |
| Source note | uspto-grants-1998_07 |