HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739810Generated: October 25, 2026
Ethyl benzoylformate → N-(1-benzyl-4-piperidinyl)phenyl-glyoxylic acid amide
https://huagongshe.com/reaction/1739810
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl benzoylformate | HCID 15349 | — |
| Reactant | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(1-benzyl-4-piperidinyl)phenyl-glyoxylic acid amide | HCID 11120838 | 81.4% |
Reaction Steps
Added to 4.28 g of ethyl phenylglyoxylate were 9.12 g of 4-amino-1-benzylpiperidine. The mixture was heated and stirred at 120° C. for 3 hours on an oil bath. Thereafter, ethanol formed was distilled off under reduced pressure, and the residue was purified by column chromatography on silica gel, thereby obtaining 6.3 g (yield: 81.4%) of N- (1-benzyl-4-piperidinyl)phenyl-glyoxylic acid amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05968956 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-8f477e3b0b734482a249820ee94a5696 |
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| Source note | uspto-grants-1999_10 |
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