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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520840Generated: October 30, 2026

Water → 6-Bromo-4-hydroxy-3-phenoxyquinolin-2(1H)-one

https://huagongshe.com/reaction/520840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantMethyl 5-bromo-2-(2-phenoxyacetamido)benzoateHCID 7765744—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-4-hydroxy-3-phenoxyquinolin-2(1H)-oneHCID 86715444—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 5-bromo-2-(2-phenoxyacetamido)benzoate (7.28 g, 20.0 mmol, Intermediate 5: step a) in tetrahydrofuran (215 mL) at −78° C. was added potassium bis(trimethylsilyl)amide (0.5 M solution in toluene, 118.7 mL, 59.37 mmol) over 7 minutes. The mixture was stirred at −78° C. for 5 minutes and 0° C. for 1.5 hours. The resulting cold solution was quenched with water. The white solid formed was completely dissolved by addition of excess water. The aqueous phase was washed once with EtOAc and then acidified by slow addition of 2 N aqueous HCl solution (kept pH above 2). The off-white precipitate formed was filtered and dried in the air overnight and at 40° C. for 1 hour to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328095B2
Source datasetuspto-grants-2016_05
ORD IDord-c8032877c4bc4c1995aa4c6690107a70
Source noteuspto-grants-2016_05