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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118640Generated: October 31, 2026

HCID 20192806, compound → HCID 86741665, compound

https://huagongshe.com/reaction/2118640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20192806HCID 20192806—
ReactantHCID 178418361HCID 178418361—
CatalystPyridineHCID 1049—
ProductHCID 86741665HCID 86741665—

Reaction Steps

5 g of N-(3cyclohex-1-en-1-yl-propynyl)-N-methyl-N-(1-naphthylmethyl)amine are hydrogenated in absolute pyridine using 750 mg Pd/BaSO4 as catalyst at room temperature and normal pressure, until the calculated amount of hydrogen is taken up. The reaction mixture is filtered and the pyridine removed in a vacuum. The residue is chromatographed on silica-gel using benzene/ethylacetate (9:1) to yield the title compound in free base form as an oil after evaoporating the appropriate fractions,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04680291
Source datasetuspto-grants-1987_07
ORD IDord-560b40c35afb4f7cb0a22207d21b566e
Source noteuspto-grants-1987_07