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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849216Generated: October 26, 2026

4-(Benzyloxy)-2-methylaniline → 1-(2-Methyl-4-benzyloxyphenyl)-4-[(2-hydroxyethyl)amino]-6-beta,beta,beta-trifluoroethoxy-2,3-dihydropyrrolo[3,2-c]quinoline

https://huagongshe.com/reaction/849216

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Benzyloxy)-2-methylanilineHCID 16773053—
Reactant4-Oxo-6-beta,beta,beta-trifluoroethoxy-2,3,4,5-tetrahydrofuro[3,2-c]quinolineHCID 19369843—
SolventWaterHCID 962—
SolventDiethylene GlycolHCID 8117—
Product1-(2-Methyl-4-benzyloxyphenyl)-4-[(2-hydroxyethyl)amino]-6-beta,beta,beta-trifluoroethoxy-2,3-dihydropyrrolo[3,2-c]quinolineHCID 1936983486%

Reaction Conditions

Temperature250 °C

Reaction Steps

4-Oxo-6-β,β,β-trifluoroethoxy-2,3,4,5-tetrahydrofuro[3,2-c]quinoline(5.7 g, 20.0 mmol) was dissolved in diethylene glycol(70 ml) and crude 4-benzyloxy-2-methyl aniline(5.6 g, 26.0 mmol) was added. The reaction mixture was refluxed at 250° C. for 15 hours. The reaction mixture was dissolved in water, extracted with dichloromethane, and the organic layer was washed with water for 3 times. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography(ethyl acetate:dichloromethane=1:1) to obtain 4.5 g of desired compound as solid in 47% of yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011044
Source datasetuspto-grants-2000_01
ORD IDord-eac70824543a4d88831844bc2ef6e005
Source noteuspto-grants-2000_01