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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109618Generated: October 31, 2026

6-Nitroindoline → 1-(1-Methyl(4-piperidyl))-6-nitroindoline

https://huagongshe.com/reaction/2109618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-NitroindolineHCID 29757—
Reactant1-Methyl-4-piperidoneHCID 74049—
ReactantSodium BicarbonateHCID 516892—
Solvent1,1-DichloroethaneHCID 6365—
Product1-(1-Methyl(4-piperidyl))-6-nitroindolineHCID 18796623—

Reaction Steps

6-Nitroindoline (5 g) was dissolved in 200 mL of dichloroethane. N-Methyl-4-piperidone (5 g) was added to the mixture, followed by NaHB(OAc)3 (12 g) and 1 mL of glacial ACOH. The mixture was stirred at RT overnight. A saturated NaHCO3 (200 mL) solution was added to the reaction mixture and stirred for 1 h. The resulting mixture was separated by separation funnel. The organic layer was extracted once with saturated NaHCO3 solution and once with brine. The resulting organic layer was dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel with 2:1 EtOAc:MeOH to afford orange oil. MS: 262 (M+1). Calc'd. for C14H19N3O2−261.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514564B2
Source datasetuspto-grants-2009_04
ORD IDord-0e5aa75c1dcf4c0cbb03b087009a6500
Source noteuspto-grants-2009_04