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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409987Generated: October 30, 2026

Potassium Cyanide → HCID 86703304, compound

https://huagongshe.com/reaction/2409987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantHCID 86703305HCID 86703305—
SolventEthanol tetrahydrofuran waterHCID 18504229—
ProductHCID 86703304HCID 8670330488.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-[6-(bromomethyl)pyridin-2-ylmethyl]-6-methoxy-2-phenyl-1H-indole (1.37 g) in water/ethanol/tetrahydrofuran (4 mL/16 mL/4 mL) was added potassium cyanide (263 mg), and the mixture was stirred at 80° C. for 13.5 hours. The reaction mixture was left to be cooled and concentrated under reduced pressure. To the residue was added water, followed by extraction with dichloromethane. The organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (1.05 g). 1H-NMR (CDCl3) δ ppm: 3.86 (3H, s), 3.95 (2H, s), 4.39 (2H, s), 6.76 (1H, dd, J=2.3, 8.5 Hz), 6.91 (1H, d, J=2.3 Hz), 7.04 (1H, d, J=7.8 Hz), 7.23 (1H, d, J=7.5 Hz), 7.30-7.39 (2H, m), 7.39-7.49 (2H, m), 7.50-7.61 (3H, m), 8.05 (1H, br s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815903B2
Source datasetuspto-grants-2014_08
ORD IDord-814804ebc6814fb19737e051d4706e6b
Source noteuspto-grants-2014_08