HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tribromoacetaldehyde → 2-(Bromomethyl)-6-methoxyquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tribromoacetaldehyde | HCID 8256 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 6-Methoxyquinaldine | HCID 70648 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Bromomethyl)-6-methoxyquinoline | HCID 21618043 | 30.6% |
Reaction Steps
A solution of 10 g (57.7 mmol) of 6-methoxy-2-methylquinoline and 30 drops of pyridine in 40 mL of N,N-dimethylformamide was stirred at 60° C. while a solution of 16.21 g (57.7 mmol) of tribromoacetaldehyde in 20 mL of N,N-dimethylformamide was added over 15 min. The reaction mixture was stirred for another 2 hr and then cooled and poured onto 600 mL of ice-water. Work-up with ethyl acetate was carried out in the usual manner. The crude product was purified by flash chromatography on 800 g of silica gel, eluting with hexane-ethyl acetate (4:1) afforded 4.45 g (30.6%) of the title compound as a violet solid. An analytical sample was obtained by recrystallization from ethanol to give colorless crystals, mp 103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05434186 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-05f640d1166041ebbf0d4aa9e957cf61 |
| Source note | uspto-grants-1995_07 |