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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089792Generated: October 30, 2026

Sulfuric Acid → HCID 10802931, compound

https://huagongshe.com/reaction/1089792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantHCID 10709437HCID 10709437—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 10802931HCID 1080293151.4%

Reaction Steps

1.8 g of α-[[(3-methylbenzyl)amino]methyl]-3,4-dimethoxybenzyl alcohol was dissolved in 13.5 ml of trifluoroacetic acid, and after adding thereto 0.41 ml of conc. sulfuric acid under ice cooling, the mixture was allowed to react for 40 minutes. The reaction solution was concentrated, and subjected to azeotropic distillation with chloroform 2 times, and after adding chloroform, the mixture was basified by addition of 28% aqueous ammonia. By a separating procedure, the chloroform layer was collected, washed with water once, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was subjected to silica gel column chromatography (chloroform-methanol-28% aqueous ammonia (15:1:0.1); a material of Rf being 0.46 [Kiesel gel 60F254 plate, chloroform-methanol-28% aqueous ammonia (15:1:0.1)] was collected, recrystallized from chloroform-n-hexane, and recrystallized from the same solvent system several times, giving 870 mg of 4-(3,4-dimethoxyphenyl)-7-methyl-1,2,3,4-tetrahydroisoquinoline (m.p. 129°-131° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05079256
Source datasetuspto-grants-1992_01
ORD IDord-5b5db30e13c24e2b87c6db33463b1fc3
Source noteuspto-grants-1992_01