HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478651Generated: October 27, 2026
Formaldehyde → Piperidine, 1-methyl-4-phenyl-
https://huagongshe.com/reaction/478651
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 4-Phenylpiperidine | HCID 69873 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Catalyst | HCID 178460666 | HCID 178460666 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Piperidine, 1-methyl-4-phenyl- | HCID 202391 | — |
Reaction Steps
4-Phenylpiperidine (12.4 mmol), paraformaldehyde (24.8 mmol) and tetraisopropoxy-titanium (12.4 mmol) are suspended in 1,2-dimethoxyethane (20 ml) and warmed to 60° C. for 30 minutes and stirred at rt for one additional hour. Sodium borohydride (12.4 mmol) is added in portions and the mixture is stirred at rt for 2 hours and at 60° C. for additional 3 hours. After cooling the solvent is evaporated and the residue is dissolved in a mixture of aqueous ammonia (60 ml) and ethyl acetate and filtered carefully. The mixture is extracted three times with ethyl acetate and the combined organic phases are dried over sodium sulfate and evaporated. A pale brown oil is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06642239B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-0a06a52daf6141dd9a21c8e6cde2d981 |
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| Source note | uspto-grants-2003_11 |
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