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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710448Generated: November 1, 2026

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

https://huagongshe.com/reaction/1710448

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 6723549064.8%

Reaction Steps

A mixture of K2CO3 (7.93 g, 57.0 mmol) and 1H-indole-2,6-dicarboxylic acid diethyl ester (5.0 g, 19.14 mmol) in DMF (30 mL) was stirred at room temperature for 0.5 h. Then 2-bromo-propionitrile (3.4 mL, 38.3 mmol) in DMF (10 mL) was added. The reaction was warmed to 80° C. and kept at this temperature for 6 h. Then the reaction was cooled down to the room temperature. Most of the DMF solvent was removed in vacuo and the crude residue was extracted several times with EtOAc. The combined organic extracts were washed with brine, dried over MgSO4 and concentrated. The crude product was triturated with MeCN to give 3.9 g of 1-(cyano-methyl-methyl)-1H-indole-2,6-dicarboxylic acid diethyl ester as a white fluffy solid. The filtrate was concentrated and purification by silica gel chromatography provided 1.6 g of 1-(cyano-methyl-methyl)-1H-indole-2,6-dicarboxylic acid diethyl ester, yield 91%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790712B2
Source datasetuspto-grants-2010_09
ORD IDord-7abc3b1c62764aa3a202a7144780f25c
Source noteuspto-grants-2010_09