HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 20559864, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | HCID 20559878 | HCID 20559878 | — |
| Reactant | HCID 21389299 | HCID 21389299 | — |
| Product | HCID 20559864 | HCID 20559864 | — |
| Product | HCID 20559872 | HCID 20559872 | — |
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-(1-piperidino)-3,4-dihydronaphthalene with phenacylbromide produces 1-phenacyl-2-di-n-butylamino-3,4-dihydronaphthalene hydrobromide, 1-phenacyl-2-diamylamino-3,4-dihydronaphthalene hydrobromide and 1-phenacyl-2-(1-piperidino)-3,4-dihydronaphthalene hydrobromide, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04066659 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-afb9d7ea899641aeb27e34ecb587001a |
| Source note | uspto-grants-1978_01 |