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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659210Generated: October 31, 2026

Phenacyl bromide → HCID 20559862, compound

https://huagongshe.com/reaction/1659210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantHCID 20559878HCID 20559878—
ProductHCID 20559862HCID 20559862—
ProductHCID 20559864HCID 20559864—
ProductHCID 20559872HCID 20559872—
ProductHCID 20559876HCID 20559876—

Reaction Steps

By following the method of Example 1a the treatment of ⟦2-di-n-butylamino-3,4-dihydro-naphthalene,2-diamylamino-3,4-dihydronaphthalene, ⟧2-di-n-butylamino-3,4-dihydronaphthalene, 2-diamylamino-3,4-dihydronaphthalene, and 2-(1-piperidino)-3,4-dihydronaphthalene with phenacylbromide produces tautomeric N-[3,4-dihydro-1-(2-oxo-2-phenylethyl)-2(1H)-naphthalenylidene]-N-butyl-butanaminium bromide in equilibrium with 1-phenacyl-2-di-n-butylamino-3,4-dihydronaphthalene hydrobromide, tautomeric N-[3,4-dihydro-1-(2-oxo-2-phenylethyl)-2(1H)-naphthalenylidene]-N-pentyl-pentanaminium bromide in equilibrium with 1-phenacyl-2-diamylamino-3,4-dihydronaphthalene hydrobromide, and tautomeric 1-[3,4-dihydro-1-(2-oxo-2-phenylethyl-2(1H)-naphthalenylidene]piperidinium bromide in equilibrium with 1-phenacyl-2-(1-piperidino)-3,4-dihydronaphthalene hydrobromide, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE030809
Source datasetuspto-grants-1981_12
ORD IDord-81c38011be974108904d90ec49152a60
Source noteuspto-grants-1981_12