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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633880Generated: October 31, 2026

Ethanol → 4-Ethyl-6-methoxy-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/1633880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantFormaldehydeHCID 712—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(3-Methoxyphenyl)butan-1-amineHCID 14528073—
SolventFormic AcidHCID 284—
Product4-Ethyl-6-methoxy-1,2,3,4-tetrahydroisoquinolineHCID 18680073—

Reaction Steps

A solution of 2-(3-methoxyphenyl)-1-butanamine (25 g, 131 mmol, prepared according to the procedure described in J. Med. Chem. 1990, 33, 153-160) in formic acid (120 mL) at room temperature was treated with paraformaldehyde (4.18 g, 131 mmol), stirred for 16 hours, treated with 25% KOH (30 mL) and ethanol (100 mL), and refluxed for 2.5 hours. The mixture was cooled to room temperature, extracted with dichloromethane, and the combined extracts were dried (MgSO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with dichloromethane to provide the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06504031B1
Source datasetuspto-grants-2003_01
ORD IDord-79184d3f718c4a2398fdadd987c32f79
Source noteuspto-grants-2003_01