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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359004Generated: November 1, 2026

Hydrogen Bromide → 4-(2-Fluoro-4-nitrophenoxy)-7-hydroxy-6-methoxyquinoline

https://huagongshe.com/reaction/2359004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant7-(Benzyloxy)-4-(2-fluoro-4-nitrophenoxy)-6-methoxyquinolineHCID 22935410—
SolventDiethyl EtherHCID 3283—
Product4-(2-Fluoro-4-nitrophenoxy)-7-hydroxy-6-methoxyquinolineHCID 13617570186%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685971B2
Source datasetuspto-grants-2014_04
ORD IDord-8dc2a7f4f6bb445a933a5f0cb23e6335
Source noteuspto-grants-2014_04