HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-bromoindoline → 1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-bromoindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-bromoindoline | HCID 22037889 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-bromoindole | HCID 22038188 | 482.4% |
Reaction Steps
1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-bromoindoline (0.1 g) was dissolved in chloroform (27 ml). After adding manganese dioxide (2.75 g), the resultant mixture was heated under reflux for 4 hr. Then manganese dioxide was filtered off and the filtrate was concentrated under reduced pressure to give the title compound (0.480 g) as a yellow oil (yield: 96.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071201B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-6b87a79f9fe34323bdf1bb84914aa04a |
| Source note | uspto-grants-2006_07 |