Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36846Generated: October 25, 2026

Water → Pyrimidine-2,4,5-triol

https://huagongshe.com/reaction/36846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantUracilHCID 1174—
ReactantPyrimidineHCID 9260—
ReactantBromineHCID 24408—
ProductPyrimidine-2,4,5-triolHCID 73268—

Reaction Steps

According to the synthetic method shown in Scheme A, above, bromine is added dropwise to an ice-cooled solution or suspension of a pyrimidine-2,4(1H,3H)-dione derivative of formula (III) in water until the solution or suspension is colored pale yellow. The pyrimidine-2,4(1H,3H)-dione derivatives of formula (III) are prepared, for example, by the methods described in Heterocyclic Compounds 16, The pyrimidine supplement II, D. J. Brown, An Interscience Publication, John Willy & Sons, New York, 1985, Table LVIII, page 728. To the resulting pale yellow solution or suspension is added carefully an ice cold saturated aqueous NaHCO3 solution. The resulting reaction mixture is refluxed, the solvent is removed and the residue is recrystallized from an appropriate solvent or chromatographed over silica-gel to give a 5-hydroxyprimidine-2,4(1H,3H)-dione derivative of formula (IV).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05418231
Source datasetuspto-grants-1995_05
ORD IDord-dfa4a8f2f7244247bf8a9676065aef98
Source noteuspto-grants-1995_05