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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089805Generated: November 1, 2026

Sulfuric Acid → 4-(6-Fluoro-3,4-dimethoxyphenyl)-7,8-dimethoxy-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/1089805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium AcetateHCID 517045—
Reactantalpha-[[(2,3-Dimethoxybenzyl)amino]methyl]-6-fluoro-3,4-dimethoxybenzyl alcoholHCID 14719568—
SolventTrifluoroacetic acidHCID 6422—
Product4-(6-Fluoro-3,4-dimethoxyphenyl)-7,8-dimethoxy-1,2,3,4-tetrahydroisoquinolineHCID 1995970098.9%

Reaction Steps

α-[[(2,3-dimethoxybenzyl)amino]methyl]-6-fluoro-3,4-dimethoxybenzyl alcohol (1.0 g) was dissolved in 7 ml of trifluoroacetic acid, and after adding thereto under ice cooling, conc. sulfuric acid (0.25 ml), the mixture was stirred for 40 minutes. 0.72 g of sodium acetate was added to the reaction mixture, and the mixture was concentrated. To the residue was added chloroform and water, and the mixture was basified by addition of conc. aqueous ammonia under ice cooling. After the separating procedure, the chloroform layer was collected, washed with a saturated aqueous NaCl solution, and dried over anhydrous sodium sulfate. The solvent was distilled off, 0.94 g of 4-(6-fluoro-3,4-dimethoxyphenyl)-7,8-dimethoxy-1,2,3,4-tetrahydroisoquinoline was obtained as a syrupy matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05079256
Source datasetuspto-grants-1992_01
ORD IDord-b935dbfa8c3d4044ba1ef636ff143856
Source noteuspto-grants-1992_01