Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883538Generated: October 25, 2026

Orotic Acid → 2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carbonyl bromide

https://huagongshe.com/reaction/883538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOrotic AcidHCID 967—
ReactantThionyl bromideHCID 68176—
SolventWaterHCID 962—
Product2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carbonyl bromideHCID 46184730—

Reaction Conditions

Temperature30 °C

Reaction Steps

In a dry 2-necked, round bottomed flask, equipped with a magnetic stirrer and fixed with a separatory funnel, containing 10.07 ml (130 mmol) of thionyl bromide, and a water condenser, is placed 15.61 g (100 mmol) of orotic acid. Addition of the thionyl bromide is completed with heating to about 30° C. over the course of about 130 minutes. When addition of the thionyl bromide is complete the mixture is heated and stirred for an additional hour. The water condenser is then replaced with a distillation side arm condenser and the crude mixture is distilled. The crude distillate in the receiving flask is then fractionally distilled to obtain the acyl bromide, orotoyl bromide. This acyl bromide, 10.95 g (50 mmol), is put into a dry separatory funnel and combined with 100 mL of dry DCM for use in the next step of the reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236952B2
Source datasetuspto-grants-2012_08
ORD IDord-65fe582f5e70446fbda47158f107ae81
Source noteuspto-grants-2012_08