Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13424001 | HCID 13424001 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13423997 | HCID 13423997 | 67.9% |
Reaction Steps
A solution of 5 g (0.024 mole) of crude 3-(phenoxymethyl)-3-piperidinol monohydrochloride and 5 g (0.096 mole) of formic acid (88%) in 10 ml of water was treated with 3 ml (0.036 mole) of formalin (37%) and heated on a steam bath for 18 hours. The reaction mixture was diluted with water, made basic with 3N sodium hydroxide, and extracted with three 40 ml portions of methylene chloride. The extracts were combined over magnesium sulfate, filtered, and evaporated under reduced pressure to give a pale yellow oil (4.2 g). The oil was chromatographed on a 400 g column of florisol using an acetone-benzene gradient (0-2%) to elute the product. Fractions containing nearly pure product were combined and evaporated under reduced pressure. The residual oil was dissolved in acetone, treated with ethereal hydrogen chloride and allowed to stand overnight. Filtration afforded 1.8 g solid, which was recrystallized from cold acetone (charcoal pretreatment) to give 1.3 g of hydrochloride salt, m.p. 151° -152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04508724 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-0daeded458454d75a9d4becfb350e17c |
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| Source note | uspto-grants-1985_04 |
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