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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485307Generated: October 29, 2026

HCID 5354160, compound → ethyl 5-fluoro-6-(E)-furfurylideneaminooxy-1,2,3,4,5,6-hexahydro-2,4-dioxopyrimidine-5-carboxylate

https://huagongshe.com/reaction/485307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 5354160HCID 5354160—
ReactantHCID 12946261HCID 12946261—
SolventHCID 21978327HCID 21978327—
Productethyl 5-fluoro-6-(E)-furfurylideneaminooxy-1,2,3,4,5,6-hexahydro-2,4-dioxopyrimidine-5-carboxylateHCID 1331820440.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

In 450 ml of pyridine-acetone (pyridine:acetone=2:1) were dissolved 131 g (0.5 mol) of ethyl 5-fluoro-6-acetoxy-1,2,3,4,5,6-hexahydro-2,4-dioxopyrimidine-5-carboxylate and 66.5 g (0.6 mol) of (Z)-furfuraldoxime, and the solution was stirred at 60° C. for 15 hours. The solvent was evaporated under reduced pressure, and the residual oily material was poured into 3 l of ice-cooled water, and crystals precipitated were collected by filtration. The crystals were washed with water (500 ml×2), dried under reduced pressure and recrystallized from ethanol and then from ethyl acetate-hexane (7:3) to yield 63.5 g of ethyl 5-fluoro-6-(Z)-furfurylideneaminooxy-1,2,3,4,5,6-hexahydro-2,4-dioxopyrimidine-5carboxylate. m.p. 152°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04536504
Source datasetuspto-grants-1985_08
ORD IDord-96c9b1cdc9ac4d13b18b81a123f0c7ba
Source noteuspto-grants-1985_08