HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Methoxide → 6-Bromo-2-methoxyquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 6-Bromo-2-chloroquinoline | HCID 12894086 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Bromo-2-methoxyquinoline | HCID 10657538 | — |
Reaction Steps
A solution of 2-chloro-6-bromoquinoline (4.0 g) in methanol (20 cm3) was heated under reflux with sodium methoxide [made from sodium (0.5 g) and methanol (20 cm3)] for 16 hours. The solvent was removed in vacuo and the residue was partitioned between water (20 cm3) and chloroform (100 cm3). The aqueous phase was extracted with chloroform (2×30 cm3) and the dried (MgSO4) extracts were evaporated to give a solid which was recrystallised from petroleum ether (b.p. 60°-80°) to yield 2-methoxy-6-bromoquinoline, m.p. 93°-96°, (3.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04710507 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-ffea307a3b4a455b9a3563f24947804e |
| Source note | uspto-grants-1987_12 |