HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093022Generated: October 25, 2026
Hydrochloric Acid → 3-(Dimethylamino)-1-(3-methoxyphenyl)-2-methylpropan-1-one
https://huagongshe.com/reaction/2093022
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3'-Methoxypropiophenone | HCID 584765 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 3-(Dimethylamino)-1-(3-methoxyphenyl)-2-methylpropan-1-one | HCID 19360495 | — |
Reaction Steps
A mixture of 1-(3-methoxyphenyl)-1-propanone (240 g) in 2-propanol (584 ml) is stirred at ambient temperature. Dimethylamine hydrochloride (238.3 g) is added, followed by paraformaldehyde (109.5 g) and an aqueous HCl solution (26.5 ml, 35% w/w). The reaction mixture is heated to reflux temperature and stirred and refluxed for 5 hours. The reaction mixture is allowed to cool to 20° C., and water (730 ml) and toluene (146 ml) are added. The upper organic layer is discarded and an aqueous NaOH solution (50% w/w, 175.2 ml) is added to the water layer while stirring for 10 minutes and keeping the temperature below 25° C. After 10 minutes the layers are allowed to separate, the upper organic layer is isolated and washed with water (219 ml). The organic layer is isolated and concentrated to obtain 3-(dimethylamino)-1-(3-methoxyphenyl)-2-methyl-1-propanone as on oily residue (294.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440863B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-ea819724f4ec4a6fa52468a74cd08883 |
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| Source note | uspto-grants-2013_05 |
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