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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104498Generated: October 30, 2026

Methyl iodide → 3-(1-Methoxy-1-Phenylethyl)-4-Phenyl-8-(Trifluoromethyl)Quinoline

https://huagongshe.com/reaction/2104498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant1-Phenyl-1-[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]ethanolHCID 11349896—
SolventDimethylformamideHCID 6228—
Product3-(1-Methoxy-1-Phenylethyl)-4-Phenyl-8-(Trifluoromethyl)QuinolineHCID 66913189—

Reaction Steps

1-Phenyl-1-[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]ethanol (Example 39, 0.096 g, 0.243 mmol) was taken into DMF (3 mL) then NaH (0.020 g, 0.487 mmol) was added and stirred for 20 minutes. Lastly, iodomethane (0.08 mL, 1.22 mmol) was added and stirring was continued for 30 minutes. The reaction was quenched with water and extracted with ether. The combined organics were dried over magnesium sulfate and concentrated. The resulting material was purified via column chromatography using 5% ethyl acetate in hexane as the eluent. MS (ESI) m/z 408 ([M+H]+); 1H NMR (CDCl3) δ 9.59 (s, 1H), 8.01 (d, J=6.8 Hz, 1H), 7.31 (m, 3H), 7.12 (m, 5H), 7.0 (m, 2H), 6.74 (dd, J=7.5 and 1.2 Hz, 1H), 6.63 (dd, J=7.7 and 1.3 Hz, 1H), 3.06 (s, 3H), 1.8 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576215B2
Source datasetuspto-grants-2009_08
ORD IDord-4b8eeb439e5949cb8c8515e2b8b70e0c
Source noteuspto-grants-2009_08