HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55387Generated: October 27, 2026
Triethylamine → N-(2,5-dimethoxy-3,4,6-trimethylbenzyl)-N-methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamine
https://huagongshe.com/reaction/55387
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(Chloromethyl)-2,5-dimethoxy-3,4,6-trimethylbenzene | HCID 10878929 | — |
| Reactant | N-Methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamine | HCID 19957678 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2,5-dimethoxy-3,4,6-trimethylbenzyl)-N-methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamine | HCID 19957658 | 75% |
Reaction Steps
N-Methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamine (4.94 g) and 2,5-dimethoxy-3,4,6-trimethylbenzyl chloride (4.29 g) were dissolved in N,N-dimethylformamide (70 ml), and triethylamine (1.89 g) was added dropwise while stirring the mixture at room temperature. The mixture was stirred at room temperature for 16.5 hours. After the reaction, the solvent was distilled off, and water was added. The mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained crude product was purified by silica gel chromatography (eluent; ethyl acetate/benzene=1/1) to give 6.40 g of a pale-yellow solid. A portion (1.0 g) was taken therefrom and recrystallized from diisopropyl ether to give 0.62 g of the title compound (colorless crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05624961 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-f9a8a70d8a224fc19a8a03acae303de4 |
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| Source note | uspto-grants-1997_04 |
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