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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391241Generated: November 2, 2026

Formaldehyde → 4-Benzyloxy-2,6-diethyl-1,2,3,6-tetramethylpiperidine

https://huagongshe.com/reaction/1391241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Benzyloxy-2,6-diethyl-2,3,6-trimethylpiperidineHCID 21330333—
SolventFormic AcidHCID 284—
Product4-Benzyloxy-2,6-diethyl-1,2,3,6-tetramethylpiperidineHCID 21330412—

Reaction Steps

To 1.0 g of 4-benzyloxy-2,6-diethyl-2,3,6-trimethylpiperidine (Compound 95 - prepared as described in Preparation 5) were added 0.52 g of formic acid and 1.22 g of 37% formalin at 0°-5° C. The mixture was stirred at room temperature and then refluxed by heating for 3 hours. When the reaction was complete, the reaction mixture was adjusted to a pH value of 8.0 by addition of a 5% aqueous solution of sodium bicarbonate; the mixture was then extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulphate and the solvent was removed by evaporation under reduced pressure. The residue was purified by column chromatography on silica gel using benzene as eluent; the resulting product was then distilled under reduced pressure, giving 0.6 g of Compound 100 as a pale yellow liquid (bp 132°-135° C./0.2 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04141883
Source datasetuspto-grants-1979_02
ORD IDord-5dc4240cda274e868d1d4a54c0cb6af9
Source noteuspto-grants-1979_02