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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702012Generated: October 29, 2026

Cyanogen Bromide → 1-(4-Chlorophenyl)-1'-cyanospiro[indoline-3,4'-piperidine]

https://huagongshe.com/reaction/1702012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine]HCID 12801589—
SolventDichloromethaneHCID 6344—
Product1-(4-Chlorophenyl)-1'-cyanospiro[indoline-3,4'-piperidine]HCID 12801611—

Reaction Steps

A mixture of 0.95 g of 1-(4-chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine] (Example 2), 0.42 g of cyanogen bromide and 1 g of potassium carbonate in 25 ml of dichloromethane is stirred at ambient temperature for two hours. The reaction mixture is filtered and the filtrate concentrated to dryness leaving an oily residue which is crystallized from an acetone-hexane mixture leaving colorless crystals, mp 178.5°-180° C. of 1-(4-chlorophenyl)-1'-cyanospiro[indoline-3,4'-piperidine].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379932
Source datasetuspto-grants-1983_04
ORD IDord-805c251af0a549008fc5e0924b014105
Source noteuspto-grants-1983_04