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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442338Generated: October 27, 2026

Sodium Cyanide → Ethyl 6-cyano-4-hydroxycinnolin-3-yl carboxylate

https://huagongshe.com/reaction/442338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178470447HCID 178470447—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductEthyl 6-cyano-4-hydroxycinnolin-3-yl carboxylateHCID 178470443—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of ethyl 6-amino-4-hydroxycinnolin-3-yl carboxylate (1.164 g.) in water (10 ml.) and concentrated hydrochloric acid (1.0 ml.) was stirred at 0° C. in an ice-salt bath, and a solution of sodium nitrite (0.5 g.) in water (3 ml.) was added during 5 minutes, maintaining the temperature at 0°-5° C. The mixture was stirred at 0° C. for 10 minutes, and this mixture was then added dropwise to a stirred solution of cuprous cyanide (0.54 g.) and sodium cyanide (0.6 g.) in water (4 ml.), heated at 60°-70° C. on a steam bath. The mixture was heated under reflux for 30 minutes. The brown solid which was precipitated was filtered off, washed thoroughly with water and dried as much as possible on the filter. The crude product was extracted with boiling ethanol (2 × 100 ml.), and the combined extracts were filtered and the filtrate evaporated under reduced pressure. The residue was applied to a column of silica (30 g., Kieselgel 60). Elution with a mixture containing 15% v/v of ethanol and 85% v/v of chloroform yielded ethyl 6-cyano-4-hydroxycinnolin-3-yl carboxylate, m.p. 259°-261° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04045439
Source datasetuspto-grants-1977_08
ORD IDord-f6cb46640c2a4da89c6b435ac2fdf341
Source noteuspto-grants-1977_08