Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | HCID 3059028 | HCID 3059028 | — |
| Reactant | Fumarate | HCID 5460307 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 3061539 | HCID 3061539 | 75.9% |
Reaction Steps
To a suspension of 10.2 g of 1-(4-methoxyphenyl) 3-(4-piperidyl) 1-propanone in 130 ml of dry tetrahydrofurane, maintained at 5° C. and under a nitrogen atmosphere, 2.8 g of lithium aluminum hydride are added in small portions. When the addition is complete, the reaction mixture is heated to 60° C. over five hours, then cooled to 0° C. Then, while maintaining this temperature, 25.2 ml of water are added very slowly. The mineral products are filtered and washed twice with 50 ml of hot methylenechloride. The collected organic solutions are concentrated by evaporation of the solvent. The oil obtained is dissolved in 150 ml of isopropanol and treated with 7.4 g of fumaric acid. In this manner, 7.8 g of 1-(4-methoxyphenyl) 3-(4-piperidyl) 1-propanol in the form of its fumarate are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04294841 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-57cbfb725d784eb6803edd7df6815bb6 |
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| Source note | uspto-grants-1981_10 |
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