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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759548Generated: November 1, 2026

Isoamyl Nitrite → HCID 13041128, compound

https://huagongshe.com/reaction/1759548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantTetrafluoroboric acidHCID 28118—
ReactantHCID 13041126HCID 13041126—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductHCID 13041128HCID 13041128—

Reaction Steps

A solution of 12.0 g of ethyl 6-amino-1-ethyl-1,4-dihydro-7-methoxy-4-oxo-1,8-naphthyridine-3-carboxylate in 120 ml of ethanol and 60 ml of aqueous 42% tetrafluoroboric acid was cooled to 0° C. To the solution kept at 0°-3° C. was added 6.0 g of isoamyl nitrite. The mixture was stirred for 30 minutes at the same temperature, and then diluted with 600 ml of ether to give a precipitate which was collected and washed with ether to give 12.8 g of 3-ethoxycarbonyl-1-ethyl-1,4-dihydro-7-methoxy-4-oxo-1,8-naphthyridine-6-diazonium tetrafluoroborate, decomposing at 142°-147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04341784
Source datasetuspto-grants-1982_07
ORD IDord-2dd85bf068844724adfcbe75a67e13db
Source noteuspto-grants-1982_07