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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655222Generated: October 30, 2026

6-Bromo-7-fluoroquinoline → (7-Fluoro-quinolin-6-yl)-acetic acid tert-butyl ester

https://huagongshe.com/reaction/655222

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-7-fluoroquinolineHCID 14548343—
ReactantHCID 178476297HCID 178476297—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product(7-Fluoro-quinolin-6-yl)-acetic acid tert-butyl esterHCID 6853460663%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 6-bromo-7-fluoro-quinoline (1.04 g, 4.6 mmole) in tetrahydrofuran (1 mL) was added a solution of tert-butylzincbromide acetate (20 mL, 10.4 M in tetrahydrofuran) followed by Pd(PPh3)4 (0.58 g, 0.5 mmole). The mixture was heated in a microwave reactor for 35 min at 120° C. The reaction mixture was quenched with a saturated ammonium chloride (60 mL), and extracted with ethyl acetate. The organic layer was dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified by column chromatography to afford the title compound (0.75 g, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071581B2
Source datasetuspto-grants-2011_12
ORD IDord-03ee9fde51c54e7ebdbf98d4e677d56a
Source noteuspto-grants-2011_12