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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050404Generated: October 30, 2026

Trifluoroacetic anhydride → HCID 118598640, compound

https://huagongshe.com/reaction/1050404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 118599043HCID 118599043—
SolventDimethylformamideHCID 6228—
ProductHCID 118598640HCID 118598640—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a 0° C. cooled solution of 5-bromo-2-(ethoxycarbonyl)pyrimidine 1-oxide (3, 0.62 g, 2.5 mmol) in dimethylformamide (6 mL), trifluoroacetic anhydride (3.1 g, 15 mmol) was added dropwise. The reaction mixture was heated at 50° C. for 18 h. TLC showed consumption of starting material and solvent was removed under reduced pressure. The residue was triturated with methanol (2 mL) and filtered. The solid was washed with diethyl ether and dried under reduced pressure to afford ethyl 5-bromo-6-oxo-1,6-dihydropyrimidine-2-carboxylate (4) as off white solid. Yield: 0.21 g, 34%; MS (ESI) m/z 245.09 [M−1]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382248B2
Source datasetuspto-grants-2016_07
ORD IDord-cd5cab4f752846e0be421896c13218c7
Source noteuspto-grants-2016_07