HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613192Generated: October 25, 2026
Potassium Carbonate → 2-methyl-2-[N-(3,4-methylenedioxybenzyl)-N-methylamino]propanol
https://huagongshe.com/reaction/1613192
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,3-Benzodioxole, 5-(chloromethyl)- | HCID 88713 | — |
| Reactant | 2-Methyl-2-methylamino-1-propanol | HCID 422780 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-methyl-2-[N-(3,4-methylenedioxybenzyl)-N-methylamino]propanol | HCID 54486224 | 58% |
Reaction Steps
A mixture of 2-methyl-2-methylaminopropanol (1.5 g), 3,4-methylenedioxybenzyl chloride (2.5 g) and potassium carbonate (2 g) in acetonitrile (50 ml) was heated under reflux for 4 hours and evaporated. The residue was partitioned between ether and 2M hydrochloric acid and the acidic layer was washed with methylene chloride, basified with 10% aqueous sodium carbonate solution and extracted into methylene chloride. The organic extract was dried over magnesium sulphate and evaporated to give essentially pure 2-methyl-2-[N-(3,4-methylenedioxybenzyl)-N-methylamino]propanol as a yellow oil (2.0 g, 58%) which was used directly in Example 34. A small portion of this product was dissolved in ether and the solution was treated with excess saturated ethereal hydrogen chloride and evaporated. The residue was triturated with acetone/ethyl acetate to give the title compound as a colourless solid, m.p. 157°-159°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05192765 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-918dbfc0cb474489870cd382c91a5f79 |
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| Source note | uspto-grants-1993_03 |
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