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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290177Generated: October 30, 2026

rel-(3R,5S)-3,5-Dimethylpiperidine → 5-[1-(4-Chlorophenoxy)-2-methylprop-2-yl]-2-(cis)-(3,5-dimethylpiperidin-1-ylmethyl)-5-methyl-tetrahydrofuran

https://huagongshe.com/reaction/2290177

Reaction equation

Participants

RoleNameHCIDCharge
Reactantrel-(3R,5S)-3,5-DimethylpiperidineHCID 641101—
Reactant2-Bromomethyl-5-[1-(4-chlorophenoxy)-2-methylprop-2-yl]-5-methyl-tetrahydrofuranHCID 13563466—
SolventDiethyl EtherHCID 3283—
Product5-[1-(4-Chlorophenoxy)-2-methylprop-2-yl]-2-(cis)-(3,5-dimethylpiperidin-1-ylmethyl)-5-methyl-tetrahydrofuranHCID 1360301345%

Reaction Steps

16 g (0.044 mole) of 2-bromomethyl-5-[1-(4-chlorophenoxy)-2-methylprop-2-yl]-5-methyl-tetrahydrofuran are stirred together with 11 g (0.097 mole) of cis-3,5-dimethylpiperidine at a bath temperature of 140° C. for about 14 hours. The resulting reaction mixture is taken up in ether and the mixture is washed several times with water, dried over sodium sulphate and concentrated in vacuo. The oily residue is purified by column chromatography (silica gel 60, ether-petroleum ether 1:1). 7.8 g (45% of theory) of 5-[1-(4-chlorophenoxy)-2-methylprop-2-yl]-2-(cis)-(3,5-dimethylpiperidin-1-ylmethyl)-5-methyl-tetrahydrofuran of refractive index nD20 1.5049 are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04615725
Source datasetuspto-grants-1986_10
ORD IDord-733caa8141114fdf9e227d0e70dd19f5
Source noteuspto-grants-1986_10