HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 4-(2-Fluoro-4-nitrophenoxy)-7-hydroxy-6-methoxyquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 7-(Benzyloxy)-4-(2-fluoro-4-nitrophenoxy)-6-methoxyquinoline | HCID 22935410 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(2-Fluoro-4-nitrophenoxy)-7-hydroxy-6-methoxyquinoline | HCID 136175701 | 86% |
Reaction Steps
7-Benzyloxy-4-(2-fluoro-4-nitro-phenoxy)-6-methoxy-quinoline (2.75 g, 6.54 mmol) was added slowly in portion into hydrobromic acid solution (33% in acetic acid, 45 ml). The mixture was stirred at room temperature for 2 hours, then poured into diethyl ether (300 ml). The precipitate was filtered and washed with diethyl ether. The solid hydrobromide salt was stirred in the mixture of sodium acetate aqueous solution (10%, 60 ml) and ethyl acetate (15 ml) for 1 day. The precipitate was filtered, washed with water and dried to give 1.82 g of product [G]. Yield: 86%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08685971B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-8dc2a7f4f6bb445a933a5f0cb23e6335 |
| Source note | uspto-grants-2014_04 |