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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748243Generated: October 29, 2026

Potassium Carbonate → diethyl 1-(1-cyanoethyl)-1H-indole-2,6-dicarboxylate

https://huagongshe.com/reaction/1748243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-BromopropionitrileHCID 140538—
ReactantDiethyl 1H-indole-2,6-dicarboxylateHCID 44754779—
SolventDimethylformamideHCID 6228—
Productdiethyl 1-(1-cyanoethyl)-1H-indole-2,6-dicarboxylateHCID 6723549091.6%

Reaction Steps

A mixture of K2CO3 (7.9 g, 57.4 mmol) and diethyl 1H-indole-2,6-dicarboxylate (Intermediate A, 5.0 g, 19.1 mmol) in DMF (30 mL) is stirred at room temperature for 30 min. A solution of 2-bromo-propionitrile (3.4 mL, 38.3 mmol) in DMF (10 mL) is added. The reaction mixture is warmed to 80° C. for 6 h and then cooled to room temperature and stirred for another 16 h. Solvent is removed and the residue is partitioned between EtOAc and water. The organic layer is separated, dried and concentrated to afford crude compound which is purified by flash column chromatography using EtOAc in hexanes followed by trituration with acetonitrile to afford the title compound (5.5 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150577B2
Source datasetuspto-grants-2015_10
ORD IDord-b6d32dc7d089434fa5e652930a62abb3
Source noteuspto-grants-2015_10