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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388176Generated: October 30, 2026

Pyridine → (1R,2S,5R)-5-Methyl-N-[3-(2-methylphenoxy)propyl]-2-(propan-2-yl)cyclohexane-1-carboxamide

https://huagongshe.com/reaction/388176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTetrahydrofuranHCID 8028—
Reactant2-PhenoxyethanamineHCID 15651—
ReactantCyclohexanecarbonyl chloride, 5-methyl-2-(1-methylethyl)-HCID 13734319—
Product(1R,2S,5R)-5-Methyl-N-[3-(2-methylphenoxy)propyl]-2-(propan-2-yl)cyclohexane-1-carboxamideHCID 67299849—

Reaction Steps

In a 25 mL round bottom flask, fitted with magnetic stirrer, 10 mL of tetrahydrofurane, 6.0 mmol (1.5 eq.) of pyridine and 3.33 mmol of 2-phenoxyethanamine were added. p-Menthane carboxylic acid chloride (4.0 mmol) were added and the mixture was stirred at room temperature for 16 hours, over night. The reaction mixture was extracted with MTBE and HCl (1N in water). The organic layer was washed with NaOH (1N in water), dried over MgSO4 and concentrated. The crude product was purified by column chromatography or crystallized from MtBE and Hexane under dry ice cooling.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377422B2
Source datasetuspto-grants-2013_02
ORD IDord-594f5c5ebda648ef93722bcda216392a
Source noteuspto-grants-2013_02