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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557357Generated: October 27, 2026

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

https://huagongshe.com/reaction/557357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-NitroindolineHCID 29757—
Reactant1-Methyl-4-piperidoneHCID 74049—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
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 12 g NaBH(OAc)3 and 1 mL of glacial ACOH. The mixture was stirred at RT overnight. Saturated NaHCO3 solution (200 mL) 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 an orange oil. MS: 262 (M+1). Calc'd. for C14H19N3O2—261.32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058445B2
Source datasetuspto-grants-2011_11
ORD IDord-aa1e7116ae65491cb0198d5e691811d8
Source noteuspto-grants-2011_11