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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660352Generated: October 30, 2026

Sodium Hydroxide → 6-Chloro-1'-methylspiro[indoline-3,4'-piperidine]

https://huagongshe.com/reaction/1660352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantLithiumHCID 3028194—
Reactant4-(4-Chloro-2-fluorophenyl)-4-cyano-1-methylpiperidineHCID 13065321—
ReactantHCID 23689305HCID 23689305—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product6-Chloro-1'-methylspiro[indoline-3,4'-piperidine]HCID 12801617—

Reaction Steps

To a refluxing suspension of lithium triethoxyaluminum hydride (prepared by dropping 12 ml of absolute ethyl alcohol carefully into a cooled slurry of 4.9 g of lithium aluminumhydride in 150 ml of glyme) is added over a 30 minute span a mixture of 8.1 g of 4-(4-chloro-2-fluorophenyl)-4-cyano-1-methylpiperidine in 80 ml of glyme. After total addition, stirring is continued at reflux for 72 hours. Thereafter, the mixture is permitted to cool before successively adding 5 ml of water, 5 ml of a 15% aqueous sodium hydroxide solution and 15 ml of water effecting a precipitate. The precipitate is collected by filtration followed by repeated washings with warm methylene chloride. The filtrate, combined with the washings, is successfully washed with water, dried and evaporated to dryness leaving a white crystalline solid. The solid is recrystallized from an acetone-pentane mixture to provide fine needles, mp 172°-173° C. of 6-chloro-1'-methylspiro[indoline-3,4'-piperidine].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307235
Source datasetuspto-grants-1981_12
ORD IDord-5f1f7a24ccc6400d87dc8d3a21af1311
Source noteuspto-grants-1981_12