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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284455Generated: November 1, 2026

Piperidin-3-ylmethanol → HCID 13422591, compound

https://huagongshe.com/reaction/1284455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-3-ylmethanolHCID 107308—
ReactantHCID 13422590HCID 13422590—
CatalystPotassium IodideHCID 4875—
SolventEthanolHCID 702—
ProductHCID 13422591HCID 13422591100%

Reaction Steps

30.3 g (0.1 mol) of 4-chloromethyl-2-[1-(4-chlorophenyl)-2-methyl-prop-2-yl]-2-methyl-1,3-dioxolane, 23 g (0.2 mol) of 3-hydroxymethylpiperidine and 0.1 g of potassium iodide in 100 ml of ethanol are heated at 150° C. under pressure (2 bar) for 15 hours. For working up, the solvent is removed in vacuo, the residue is taken up in 100 ml of methylene chloride, the mixture is washed twice with 100 ml of water each time and dried over sodium sulphate and the solvent is removed again in vacuo. 38 g (100% of theory) of 2-[1-(4-chlorophenyl)-2-methyl-prop-2-yl]-4-[(3-hydroxymethylpiperidin-1-yl)-methyl]-2-methyl-1,3-dioxolane of refractive index n20 1.5226 are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04563447
Source datasetuspto-grants-1986_01
ORD IDord-977c5dd771844bb683a23d08b3b3b4d7
Source noteuspto-grants-1986_01