HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → 2-Phenyl-1,2,3,4-tetrahydroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | HCID 178419663 | HCID 178419663 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Phenyl-1,2,3,4-tetrahydroquinoline | HCID 10752915 | — |
Reaction Steps
By the 3-step method of Preparation E, substituting 1M phenyllithium in ether for the benzylmagnesium bromide solution, quinoline (25 g, 0.194 mol) was converted to present title product, 22.4 g, as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04738972 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-14a187deddf0425e914ed4619b3b5fe1 |
| Source note | uspto-grants-1988_04 |