HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680876Generated: October 31, 2026
Acetic Acid → 1-(2H-1,3-Benzodioxol-5-yl)-2-methylpropan-2-amine
https://huagongshe.com/reaction/1680876
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | HCID 23454854 | HCID 23454854 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | HCID 178418361 | HCID 178418361 | — |
| Product | 1-(2H-1,3-Benzodioxol-5-yl)-2-methylpropan-2-amine | HCID 13020598 | 72.2% |
Reaction Steps
A mixture of 0.8 g of 1-(3,4-methylenedioxyphenyl)-2-methyl-2-nitropropane, 100 mg of platinum dioxide, one ml of acetic acid and 20 ml of 1,2-dimethoxyethane is shaken at 60°-70° C. for 18 hours in hydrogen gas atmosphere under elevated pressure (initial pressure: 80 atmospheric pressures). After the reaction, the insoluble materials are removed by filtration, and the filtrate is evaporated to remove solvent. The residue is dissolved in ethyl acetate, and the solution is extracted with 5% hydrochloric acid. The extract is alkalized with potassium carbonate, and then extracted with ethyl acetate. The extract is washed with a saturated sodium chloride solution, dried and then evaporated to remove solvent. The residue (oil) is distilled at 100°-120° C. (bath temperature) under reduced pressure (0.04 mm Hg). 0.5 g of α,α-dimethyl-3,4-methylenedioxyphenethylamine are thereby obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04276304 |
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| Source dataset | uspto-grants-1981_06 |
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| ORD ID | ord-77a001c3419d4ff29c5942eff6428b9c |
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| Source note | uspto-grants-1981_06 |
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