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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226473Generated: November 2, 2026

Piperidine → HCID 18965299, compound

https://huagongshe.com/reaction/2226473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 12518282HCID 12518282—
ProductHCID 18965299HCID 18965299—

Reaction Conditions

Temperature60 °C

Reaction Steps

Mix 2-chloroethyl heptyl sulfone (1.1 g, 5 mmol) and piperidine (10 mL). Stir at 60° C. overnight. Add addition piperidine (5 mL) and stir at 60° C. overnight. Cool to room temperature, partition between 5N sodium hydroxide and ethyl ether. Separate the organic phase and extract the aqueous phase with ethyl ether (2×25 mL). Combine the organic phases, dry (MgSO4) and evaporate in vacuo to yield 1.2 g orange oil which crystallizes. Purify by silica gel chromatography (ethyl acetate) to yield 930 mg. Purify again by silica gel chromatography (hexane, then 10% ethyl acetate/hexane, then 50% ethyl acetate/hexane) to yield 360 mg of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348964
Source datasetuspto-grants-1994_09
ORD IDord-12f1c175fcb544e19b75f47966ab2c05
Source noteuspto-grants-1994_09