Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-Carbethoxyphthalimide | HCID 31187 | — |
| Reactant | HCID 18462748 | HCID 18462748 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22596157 | HCID 22596157 | 39.5% |
Reaction Steps
To a stirred solution of 1-(3′,4′-dimethoxyphenyl)-2-propylpentylamine (0.40 grams, 1.60 mmol) and sodium carbonate (0.18 grams, 1.72 mmol) in a mixture of water (5 milliliters) and acetonitrile (10 milliliters) was added N-carbethoxyphthalimide (0.35 grams, 1.60 mmol). The resulting solution was stirred for 2.5 hours at room temperature, the acetonitrile was evaporated and a two phase mixture resulted. The organic phase was extracted into methylene chloride, dried over magnesium sulfate and concentrated in vacuo to afford 0.6 grams of crude product as an oil. The crude product was purified by flash chromatography (silica gel, 25% ethyl acetate/hexane) to afford 0.25 grams of the product as an oil which after a few days solidified. The white solid was dried in vacuo (60° C., <1 mm) to afford 0.24 grams of pure product as a white solid: mp 100-101° C.; 1H NMR (CDCl3) δ7.84-7.59(m, 4H), 7.27-7.02(m, 2H), 6.81-6.68(m, 1H), 5.01(d, J=12 Hz, 1H), 3.89(s, 3H), 3.84(s, 3H), 3.17-2.98(m, 1H), 1.49-0.66(m, 14H). 13C NMR (CDCl3) δ168.5, 148.7, 148.4, 133.8, 131.9, 131.8, 123.1, 121.6, 112.0, 110.7, 58.9, 55.9, 55.7, 36.2, 31.9, 31.8, 18.7, 18.1, 14.6, 14.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06429221B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-3b5346f8d66d4089babeb59593b09e9a |
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| Source note | uspto-grants-2002_08 |
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