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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720317Generated: October 31, 2026

3,4,5-Trimethoxyaniline → 5,6,7-Trimethoxy-2-methylquinoline

https://huagongshe.com/reaction/720317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxyanilineHCID 32285—
ReactantCrotonaldehydeHCID 447466—
SolventHydrochloric AcidHCID 313—
Product5,6,7-Trimethoxy-2-methylquinolineHCID 14000974—

Reaction Steps

A 6 M hydrochloric acid solution (20 mL) of 3,4,5-trimethoxyaniline (3.1 g) was heated to 100° C., to which crotonaldehyde (1.5 mL) was slowly added dropwise. The mixture was stirred for 3.5 hours as it is. After allowing the reaction mixture to cool, it was washed with ether, and the resultant water layer was alkalified with a potassium carbonate solution. After extracted with ethyl acetate, the resultant organic layer was washed with water and saturated brine and dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure, and the residue was then purified by column chromatography on silica gel (ethyl acetate:hexane=1:2 to 1:1) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135473B2
Source datasetuspto-grants-2006_11
ORD IDord-b300e19a1a534c2ab471cb29b1672e9e
Source noteuspto-grants-2006_11