Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | HCID 20559878 | HCID 20559878 | — |
| Product | HCID 20559862 | HCID 20559862 | — |
| Product | HCID 20559864 | HCID 20559864 | — |
| Product | HCID 20559872 | HCID 20559872 | — |
| Product | HCID 20559876 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE030809 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-81c38011be974108904d90ec49152a60 |
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| Source note | uspto-grants-1981_12 |
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