Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 12804791 | HCID 12804791 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Boron trifluoride | HCID 6356 | — |
| Product | HCID 13288031 | HCID 13288031 | — |
Reaction Steps
A solution of 2.60 g of 3-hydroxy-1-methyl-3-(α-phenyl-2-tolyl)pyrrolidine of Example 53, in 30 ml of acetic acid and 2 ml of BF3.ether is stirred at 50°-60° C. for 21/2 hours and 16 hours at room temperature. The mixture is diluted with 30 ml of H2O, is made alkaline with NaOH, and extracted with CH2Cl2. The CH2Cl2 solution is dried (Na2SO4) and concentrated to an oil. A portion of the oil is dissolved in 10 ml of acetic acid and stirred with 0.7 ml of H2SO4 at 55° C. for 2 hours. A solution of the resultant oil in 15 ml of acetone is heated with 1.1 g of fumaric acid for dissolving and after cooling a product is isolated and recrystallized from acetone (60 ml) to provide 1-methyl-3-(α-phenyl-2-tolyl)-3 -pyrroline fumarate, mp 131°-132.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04311703 |
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| Source dataset | uspto-grants-1982_01 |
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| ORD ID | ord-880ed9f5eac1468cadf3d39c425ecee2 |
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| Source note | uspto-grants-1982_01 |
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