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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721612Generated: November 2, 2026

4-Methylpiperidine-1-carbonyl Chloride → HCID 15308022, compound

https://huagongshe.com/reaction/1721612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylpiperidine-1-carbonyl ChlorideHCID 15221516—
ReactantHCID 19976080HCID 19976080—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventBenzeneHCID 241—
ProductHCID 15308022HCID 15308022105.2%

Reaction Steps

4-Methyl-1-piperidinecarbonyl chloride (1.18 ml, 8.01 mmol) was added under a nitrogen atmosphere at room temperature to a solution of 2-hydroxy-5-phenoxybenzonitrile (1.53 g, 7.26 mmol) and 4-dimethylaminopyridine (0.976 g, 7.99 mmol) in 50 ml of benzene and the resulting solution refluxed for 1 hour. The reaction mixture was washed with 1N HCl. The benzene layer was separated, dried (anhydrous MgSO4) and the solvent removed under reduced pressure to give 2.57 g of a white crystalline solid. Recrystallization of this solid from diisopropyl ether-hexane gave the title compound as a white crystalline solid (1.59 g, 65%), mp 54°-58° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512565
Source datasetuspto-grants-1996_04
ORD IDord-b2b323f3b7ac403686dcd2ff28d7d753
Source noteuspto-grants-1996_04