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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75348Generated: October 28, 2026

N-(2-Fluorophenyl) cinnamamide → 8-Fluoroquinolin-2(1H)-one

https://huagongshe.com/reaction/75348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Fluorophenyl) cinnamamideHCID 303250—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventChlorobenzeneHCID 7964—
Product8-Fluoroquinolin-2(1H)-oneHCID 19898674—

Reaction Conditions

Temperature125 °C

Reaction Steps

N-(2-Fluorophenyl)cinnamamide (10.5 g, 44 mmol) was dissolved in chloro-benzene (60 mL) and aluminum trichloride (29.0 g, 218 mmol, 5 eq) was added. The reaction was heated to 125° C. for 3 h and then cooled to rt over 45 min. The reaction was poured onto 300 g of ice with stirring, producing a tan solid. The solid was filtered and washed with 100 mL of water and 3×100 mL of hexanes and dried under high vacuum. The solid was extracted with 1 L of DCM and filtered to remove insoluble byproducts. The solvent was removed in vacuo to afford 8-fluoroquinolin-2(1H)-one. 1H NMR (400 MHz, CDCl3) δ ppm 10.95 (br s, 1H), 7.77 (dd, J=9.8, 1.6 Hz, 1H), 7.35 (d, J=7.8 Hz, 1H), 7.27 (ddd, J=10.2, 7.8, 1.2 Hz, 1H), 7.14 (td, J=8.0, 5.1 Hz, 1H), 6.76 (d, J=9.4 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835432B2
Source datasetuspto-grants-2014_09
ORD IDord-af76ff157f9445a5b2d640c5f613b844
Source noteuspto-grants-2014_09