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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520844Generated: October 30, 2026

Potassium bis(trimethylsilyl)amide → 6-Bromo-3-(4-chlorophenoxy)-4-hydroxyquinolin-2(1H)-one

https://huagongshe.com/reaction/520844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantMethyl 5-bromo-2-(2-(4-chlorophenoxy)acetamido)benzoateHCID 7765743—
ReactantAcetone cardiceHCID 18522661—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-3-(4-chlorophenoxy)-4-hydroxyquinolin-2(1H)-oneHCID 86715454—

Reaction Steps

To a suspension of methyl 5-bromo-2-(2-(4-chlorophenoxy)acetamido)benzoate (5.15 g, 12.9 mmol, Intermediate 7: step a) in THF (140 mL) at −78° C. was added potassium bis(trimethylsilyl)amide (0.5 M in toluene, 76.7 mL, 38.4 mmol) over 4 minutes, and the mixture was stirred for 5 minutes. The dry-ice/acetone bath was replaced an with an ice-water bath and the reaction was stirred for 1.5 hours. The reaction was then quenched with water and ethyl acetate was added. The organic layer was removed and the aqueous layer was acidified with 2 N HCl (kept pH above 2). An off-white precipitate formed which was filtered and the solid was dried overnight in the air to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328095B2
Source datasetuspto-grants-2016_05
ORD IDord-5de976759283471abfa7338119820d63
Source noteuspto-grants-2016_05