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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40182Generated: October 26, 2026

Tetrahydrofuran → Ethyl 3-(7-methoxyquinolin-4-yl)propanoate

https://huagongshe.com/reaction/40182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
Reactant4-Chloro-7-methoxyquinolineHCID 10607829—
ReactantHCID 178471816HCID 178471816—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventAmmonium HydroxideHCID 14923—
ProductEthyl 3-(7-methoxyquinolin-4-yl)propanoateHCID 67503802—

Reaction Steps

4-chloro-7-methoxyquinoline (0.35 g, 2 mmol), tri-t-butylphosphonium tetrafluoroborate (0.05 g, 0.2 mmol), and tris(dibenzylideneacetone)dipalladium (0) (0.08 g, 0.09 mmol) were combined. The reaction vessel was purged and flushed with nitrogen three times, followed by addition of 3-ethoxy-3-oxopropylzinc bromide in THF (10 mL, 5 mmol, 0.5 M). The reaction mixture was microwaved at 150° C. for 60 minutes. Upon completion, ammonium hydroxide (10 mL) was added. After 30 minutes the mixture was filtered and the filtrate was partitioned between water and ethyl acetate. Extracted with ethyl acetate (3×20 mL). The organic layers were combined, washed with brine, dried over magnesium sulfate, and concentrated. Purified by MPLC with a gradient of 20 to 50% EtOAc in CH2Cl2. (ESI, pos. ion) m/z: 354.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524900B2
Source datasetuspto-grants-2013_09
ORD IDord-2749dc371527437e9924f4eb2acea80b
Source noteuspto-grants-2013_09