Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 54189816 | HCID 54189816 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54140787 | HCID 54140787 | — |
Reaction Steps
A solution of 1-Acetyl-piperidine-4-carboxylic acid (2-oxo-2-phenyl-ethyl)-amide (40.66 g, 141 mmol), prepared as in Intermediate 2A, in 2:1 EtOH: H2O (160 mL EtOH, 80 mL H2O) is treated with 37% aqueous formaldehyde (21.1 mL, 282 mmol) and NaCHO3 (1.18 g, 14.1 mmol). The reaction mixture is stirred at 23° C. for 6 h, and the resulting precipitate is removed by filtration. The filtrate is cooled to 0° C. and diluted with H2O (100 mL), and a second crop of 1-Acetyl-piperidine-4-carboxylic acid (1-hydroxymethyl-2-oxo-2-phenyl-ethyl)-amide is obtained by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090825 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-a78564fdbc87478fa623fa830c296a49 |
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| Source note | uspto-grants-2000_07 |
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