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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464273Generated: October 30, 2026

Ethyl orthoformate → HCID 13385698, compound

https://huagongshe.com/reaction/464273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 13385676HCID 13385676—
ProductHCID 13385698HCID 13385698—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture consisting of 10 g. (0.047 mole) of 2-chloro-6-fluoro-3-hydrazinoquinoxaline and 80 ml. (0.47 mole) of triethyl orthoformate was heated under a nitrogen atmosphere with mechanical stirring in a preheated oil bath at 100° C. overnight (~16 hours). The resulting mixture was cooled to room temperature, and the precipitate which formed was subsequently recovered by means of suction filtration, washed with three-50 ml. portions of ethanol and air-dried to constant weight to ultimately afford 9.42 g. (91%) of pure 4-chloro-8-fluoro-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 310°-312° C. (decomp.). Mass Spectrum: m/e, 224, 223, 222 (P+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547501
Source datasetuspto-grants-1985_10
ORD IDord-24cd995b86ba4696a620ab2918a837fc
Source noteuspto-grants-1985_10