HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647645Generated: October 29, 2026
Toluene → Methyl 4,4-ethylenedioxy-1,2,3,4-tetrahydro-5,8-dimethoxynaphthalene-2-carboxylate
https://huagongshe.com/reaction/647645
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Methyl 5,8-dimethoxy-4-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate | HCID 12772827 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | Methyl 4,4-ethylenedioxy-1,2,3,4-tetrahydro-5,8-dimethoxynaphthalene-2-carboxylate | HCID 13264135 | 61% |
Reaction Steps
40 g of methyl rac-1,2,3,4-tetrahydro-5,8-dimethoxy-4-oxonaphthalene-2-carboxylate were added to a mixture of 800 ml of toluene, 800 ml of hexane, 30 ml of ethyleneglycol and 0.65 g of toluene-4-sulphonic acid. The mixture was heated under reflux for 24 hours using a Dean-Stark trap. The solution was cooled in an ice-bath and washed with three 124 ml portions of 10% potassium hydrogen carbonate solution and 200 ml of brine, dried and the solvent was evaporated. The residue was taken up in 200 ml of methanol at 70° C. and 0.5 g of a 50% dispersion of sodium hydride in mineral oil was added. The solution obtained was left to cool to room temperature and then cooled further in an ice-bath for 2 hours. The crystalline product was filtered off, washed with cold methanol and dried in vacuo. There were obtained 28.5 g (61%) of methyl rac-4,4-ethylenedioxy-1,2,3,4-tetrahydro-5,8-dimethoxynaphthalene-2-carboxylate in the form of colourless crystals of melting point 133°-134° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04409391 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-bd19c3ebd6274c7fb8465d1f0923285d |
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| Source note | uspto-grants-1983_10 |
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