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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478651Generated: October 27, 2026

Formaldehyde → Piperidine, 1-methyl-4-phenyl-

https://huagongshe.com/reaction/478651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant4-PhenylpiperidineHCID 69873—
ReactantSodium borohydrideHCID 4311764—
CatalystHCID 178460666HCID 178460666—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductPiperidine, 1-methyl-4-phenyl-HCID 202391—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642239B2
Source datasetuspto-grants-2003_11
ORD IDord-0a06a52daf6141dd9a21c8e6cde2d981
Source noteuspto-grants-2003_11