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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978822Generated: November 2, 2026

1H-indole-6-carbonitrile → HCID 15490886, compound

https://huagongshe.com/reaction/1978822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-indole-6-carbonitrileHCID 85146—
ReactantHCID 21201384HCID 21201384—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15490886HCID 15490886—

Reaction Steps

77 mmol of potassium tert-butylate are added to a solution of 70 mmol of 6-cyanoindole in 400 ml of tetrahydrofuran. After 10 minutes' stirring at room temperature, 70 mmol of tert-butyl 3-[(methylphenyl)sulphonyloxymethyl]-1-pyrrolidinecarboxylate in 60 ml of tetrahydrofuran are added. The reaction mixture is heated at reflux for 12 hours. After cooling and dilution with water, the solvent is removed by evaporation. The residue is extracted with dichloromethane and the organic phase is washed with water, dried and concentrated to yield the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239129B1
Source datasetuspto-grants-2001_05
ORD IDord-d858b49666934ec78072c080364123e0
Source noteuspto-grants-2001_05