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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632845Generated: November 1, 2026

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

https://huagongshe.com/reaction/1632845

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 numberUS04477667
Source datasetuspto-grants-1984_10
ORD IDord-63e7f3b021fd453a84acc1bef25d9e84
Source noteuspto-grants-1984_10