HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → 6,7-Dichloro-2,3-dimethoxy-5-(1-hydroxypropyl)-quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 6,7-Dichloro-2,3-dimethoxy-5-formylquinoxaline | HCID 10493492 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6,7-Dichloro-2,3-dimethoxy-5-(1-hydroxypropyl)-quinoxaline | HCID 10852929 | 43% |
Reaction Steps
Ethylmagnesium bromide (9.08 mL, 3M in diethyl ether) was added to a suspension of 6,7dichloro-2,3-dimethoxy-5-formylquinoxaline (3.91 g, 13.62 mmol) (Preparation 2) in dry tetrahydrofuran (200 mL) under nitrogen at room temperature. After 30 minutes, saturated sodium chloride (50 mL) was added, and the product was extracted into ethyl acetate (2×100 mL). The combined extracts were dried (MgSO4) and concentrated under reduced pressure. Purification by flash chromatography (eluting with dichloromethane) gave 6,7-dichloro-2,3-dimethoxy-5-(1-hydroxypropyl)-quinoxaline (1.86 g, 43%), as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05783572 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-62fd8c3703064ac6b36a1fb7d70848bf |
| Source note | uspto-grants-1998_07 |