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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290174Generated: October 30, 2026

3,5-Dimethylpiperidine → HCID 19864356, compound

https://huagongshe.com/reaction/2290174

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DimethylpiperidineHCID 118259—
ReactantHCID 13563467HCID 13563467—
SolventEthyl AcetateHCID 8857—
ProductHCID 19864356HCID 1986435620%

Reaction Steps

20 g (0.073 mole) of 2-bromomethyl-5-(4-chlorophenyl)-tetrahydrofuran and 25 g (0.22 mole) of 3,5-dimethylpiperidine are heated at 120° C. for 16 hours. The cooled reaction mixture is taken up in ethyl acetate and the mixture is washed twice with water, dried over sodium sulphate and concentrated in vacuo. The oily residue is purified by column chromatography (silica gel 60/ligroin-ethyl acetate 2:1/ethyl acetate). 4.5 g (20% of theory) of 2-(4-chlorophenyl)-5-(3,5-dimethylpiperidin-1-ylmethyl)-tetrahydrofuran are obtained as an oil; nD20 =1.5159.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04615725
Source datasetuspto-grants-1986_10
ORD IDord-4c6b26187b064d089dc2edeb97056827
Source noteuspto-grants-1986_10