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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790471Generated: October 26, 2026

1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-bromoindoline → 1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-bromoindole

https://huagongshe.com/reaction/1790471

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-bromoindolineHCID 22037889—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-bromoindoleHCID 22038188482.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071201B2
Source datasetuspto-grants-2006_07
ORD IDord-6b87a79f9fe34323bdf1bb84914aa04a
Source noteuspto-grants-2006_07