HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55385Generated: October 28, 2026
Triethylamine → N-(2-ethoxy-5-hydroxy-3,4,6-trimethylbenzyl)-N-methyl-2-(4-hydroxy-2-isopropyl-5-methylphenoxy)ethylamine hydrochloride
https://huagongshe.com/reaction/55385
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Ethoxy-5-hydroxy-3,4,6-trimethylbenzyl chloride | HCID 19957711 | — |
| Reactant | N-methyl-2-(4-hydroxy-2-isopropyl-5-methylphenoxy)ethylamine hydrochloride | HCID 67726891 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-ethoxy-5-hydroxy-3,4,6-trimethylbenzyl)-N-methyl-2-(4-hydroxy-2-isopropyl-5-methylphenoxy)ethylamine hydrochloride | HCID 19957679 | 5% |
Reaction Steps
N-Methyl-2-(4-hydroxy-2-isopropyl-5-methylphenoxy)ethylamine hydrochloride (10.4 g), 2-ethoxy-5-hydroxy-3,4,6-trimethylbenzyl chloride (9.15 g) and triethylamine (8.10 g) were dissolved in N,N-dimethylformamide (80 ml), and the mixture was stirred at room temperature for 4 hours. After the reaction, the solvent was distilled off and water was added. The mixture was extracted with ethyl acetate, and the extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The resulting liquid (1.0 g) was dissolved in methanol and conc. hydrochloric acid (0.2 ml) was added. The mixture was concentrated to dryness under reduced pressure. Recrystallization from ethanol-diethyl ether gave 910 mg of the title compound.
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-90fae843b7e34b32be9273363dff04aa |
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| Source note | uspto-grants-1997_04 |
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