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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247262Generated: October 30, 2026

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

https://huagongshe.com/reaction/2247262

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-NitroindolineHCID 29757—
Reactant1-Methyl-4-piperidoneHCID 74049—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
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 numberUS07687643B2
Source datasetuspto-grants-2010_03
ORD IDord-b3a6d3ec823441cfb504ad6eb877ef06
Source noteuspto-grants-2010_03