Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,2-Bis(chloromethyl)-4,5-dimethoxybenzene | HCID 10944400 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86744223 | HCID 86744223 | — |
Reaction Steps
1.33 g (11 mmol) of N-benzylmethylamine and 2.07 g (15 mmol) of potassium carbonate were suspended in 24 ml of acetone, and 2.35 g (10 mmol) of 4,5-bis(chloromethyl)veratrol was added thereto at room temperature. The mixture was stirred for 18 hours. After cooling, the precipitate was collected by filtration, washed with 10 ml of acetone and dried in air to obtain 5.03 g (purity: 53%) of a white powder of the above identified compound containing inorganic substance. This powder was dissolved in 20 ml of water. Then, the solution was adjusted to pH 2.8 with 2N hydrochloric acid and subjected to HP-20 (50 ml). Elution was conducted with water, and a fraction containing the desired product was collected. The solvent was distilled off, and 10 ml of acetone was added to the oily residue. The mixture was left to stand overnight. The precipitated crystals were collected by filtration and washed with 10 ml of acetone to obtain 720 mg of the above identified compound as colorless needle crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04958029 |
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| Source dataset | uspto-grants-1990_09 |
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| ORD ID | ord-c2480149e66249d19e5c68f965cff13f |
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| Source note | uspto-grants-1990_09 |
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