HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(3-hydroxy-6-methoxy-2,4,5-trimethylbenzyl)-N-methyl-2-(2-isopropyl-5-methylphenoxy)ethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Hydroxy-6-methoxy-2,4,5-trimethylbenzyl chloride | HCID 10921874 | — |
| Reactant | N-methyl-2-(2-isopropyl-5-methylphenoxy)ethylamine | HCID 19957700 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(3-hydroxy-6-methoxy-2,4,5-trimethylbenzyl)-N-methyl-2-(2-isopropyl-5-methylphenoxy)ethylamine | HCID 19957653 | 93.6% |
Reaction Steps
Triethylamine (7.0 ml) was added dropwise to a solution of 3-hydroxy-6-methoxy-2,4,5-trimethylbenzyl chloride (10.73 g) and N-methyl-2-(2-isopropyl-5-methylphenoxy)ethylamine (10.37 g) in N,N-dimethylformamide (60 ml) while stirring the mixture at room temperature. Immediately after the dropwise addition, heat was developed and salt was precipitated. The mixture was stirred at room temperature for 2 hours and triethylamine (2.0 ml) was added. The mixture was stirred for 1 hour. The reaction mixture was poured on ice water and extracted with ethyl acetate to give a crude product. The product was purified by silica gel chromatography (eluent; ethyl acetate/benzene=1/1) to give 18.03 g of the title compound (pale brown solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05624961 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-5203103535ef4ddfab21bf161f425d1f |
| Source note | uspto-grants-1997_04 |