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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104489Generated: October 30, 2026

Ethylene Glycol → 3-Benzyl-4-phenyl-8-(trifluoromethyl)quinoline

https://huagongshe.com/reaction/2104489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantPhenyl[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]methanoneHCID 11360909—
SolventWaterHCID 962—
Product3-Benzyl-4-phenyl-8-(trifluoromethyl)quinolineHCID 1141716754.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

Phenyl[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]methanone (Example 1, 0.244 g, 0.65 mmol) was taken into ethylene glycol (5 mL) along with hydrazine hydrate (0.3 mL) and heated at 120° C. for 2 hours. Next, a few pellets of KOH were added and reaction was heated at 180° C. for 4 hours. The reaction was allowed to cool to room temperature, where water was added and the mixture was extracted with ether and concentrated. The resulting material was purified via column chromatography using 5% ethyl acetate in hexane as the eluent to produce 0.128 g of desired product. MS (ESI) m/z 364 ([M+H]+); 1H NMR (CDCl3) δ 9.01 (s, 1H), 8.02 (d, J=7.2 Hz, 1H), 7.65 (d, J=7.6 Hz, 1H), 7.51 (m, 3H), 7.44 (m, 1H), 7.20 (m, 5H), 6.97 (m, 2H), 3.98 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576215B2
Source datasetuspto-grants-2009_08
ORD IDord-2f9bf6c7140f4b8695e533d5f20c5f82
Source noteuspto-grants-2009_08