HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590825Generated: October 31, 2026
Sulfuric Acid → 4-(3,4-Dimethoxyphenyl)-6-methyl-1,2,3,4-tetrahydroisoquinoline
https://huagongshe.com/reaction/1590825
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 86746746 | HCID 86746746 | — |
| Product | 4-(3,4-Dimethoxyphenyl)-6-methyl-1,2,3,4-tetrahydroisoquinoline | HCID 10684399 | — |
Reaction Steps
530 mg of α-[[(4-methylbenzyl)amino]methyl]-3,4-dimethoxybenzyl benzyl alcohol was dissolved in 4 ml of trifluoroacetic acid, and after adding thereto 0.12 ml of conc. sulfuric acid under ice cooling, the mixture was allowed to react for 30 minutes. The reaction solution was concentrated, and subjected to azeotropic distillation with toluene 2 times. After adding chloroform, the mixture was basified by addition of 28% aqueous ammonia. By a separating procedure, the chloroform layer was collected, was washed with water once, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was recrystallized from ethyl acetate-n-hexane, giving 490 mg of 4-(3,4-dimethoxyphenyl)-6-methyl-1,2,3,4tetrahydroisoquinoline (melting point: 94°-96° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05204468 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-0a0b12734029467da49f0dab29352613 |
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| Source note | uspto-grants-1993_04 |
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