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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441680Generated: October 25, 2026

Acetic Acid → 1-(Methylcarbonyloxy-methyl)-5-(2-decahydronaphthyl)-spiro[indoline-3,4'-piperidin]-2-one

https://huagongshe.com/reaction/1441680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-DecaloneHCID 100328—
ReactantCyano-borohydrideHCID 498716—
Reactant1-(Methoxycarbonylmethyl)-spiro[indoline-3,4'-piperidin]-2-oneHCID 59164537—
Solvent1,2-DichloroethaneHCID 11—
SolventTetrahydrofuranHCID 8028—
Product1-(Methylcarbonyloxy-methyl)-5-(2-decahydronaphthyl)-spiro[indoline-3,4'-piperidin]-2-oneHCID 68539668—

Reaction Steps

1-(Methoxycarbonylmethyl)-spiro[indoline-3,4′-piperidin]-2-one (0.013 g, 0.049 mmol) was dissolved in dry THF (1.0 mL) and dry 1,2-dichloroethane (0.3 mL). Octahydro-naphthalen-2-one (0.008 g, 0.054 mmol), glacial acetic acid (0.003 g, 0.049 mmol), MP-cyanoborohydride (Polymer support from Argonaut) (0.043 g, 0.099 mmol) were added and the reaction mixture was stirred at room temperature for 18 hrs. The mixture was then filtered, the resin washed with dichloromethane and the solvent evaporated in vacuo to yield the crude compound. The crude compound was purified via flash chromatography (5% methanol/dichloromethane) to yield the title compound as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655670B2
Source datasetuspto-grants-2010_02
ORD IDord-16b619f70a0d4189b576a82578d32524
Source noteuspto-grants-2010_02