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
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 5354160 | HCID 5354160 | — |
| Reactant | HCID 12946261 | HCID 12946261 | — |
| Solvent | HCID 21978327 | HCID 21978327 | — |
| Product | ethyl 5-fluoro-6-(E)-furfurylideneaminooxy-1,2,3,4,5,6-hexahydro-2,4-dioxopyrimidine-5-carboxylate | HCID 13318204 | 40.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04536504 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-96c9b1cdc9ac4d13b18b81a123f0c7ba |
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| Source note | uspto-grants-1985_08 |
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