Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392084Generated: October 25, 2026

Water → Ethyl 6-chloro-1-(cyanomethyl)-5-methylindole-2-carboxylate

https://huagongshe.com/reaction/392084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroacetonitrileHCID 7856—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 6-chloro-5-methyl-1h-indole-2-carboxylateHCID 21868716—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 6-chloro-1-(cyanomethyl)-5-methylindole-2-carboxylateHCID 21868765—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of ethyl 6-chloro-5-methylindole-2-carboxylate (1.5 g, 6.3 mmol) in DMF (30 mL) was added dropwise to a stirred suspension of sodium hydride (60%, 0.39 g, 10 mmol) in DMF (20 mL) at room temperature under Ar. The reaction was then cooled to 0° C. and stirred for 45 min then chloroacetonitrile (0.81 mL, 13 mmol) was added in one portion. The reaction was heated to 75° C. and stirred for 1 h. After allowing to cool to room temperature the mixture was poured into water (200 mL) and with ethyl acetate (3×100 mL). The combined organic extracts were washed with brine (1×100 mL), dried (magnesium sulfate), filtered and the solvent removed under vacuum to leave the crude product which was used immediately.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800627B1
Source datasetuspto-grants-2004_10
ORD IDord-e3e3b71823754d06b5a96a1267be853d
Source noteuspto-grants-2004_10