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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660346Generated: October 31, 2026

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

https://huagongshe.com/reaction/1660346

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 numberUS04307235
Source datasetuspto-grants-1981_12
ORD IDord-3d8ff71eec18409f94161d0178b09f19
Source noteuspto-grants-1981_12