HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050404Generated: October 30, 2026
Trifluoroacetic anhydride → HCID 118598640, compound
https://huagongshe.com/reaction/1050404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 118599043 | HCID 118599043 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 118598640 | HCID 118598640 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382248B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-cd5cab4f752846e0be421896c13218c7 |
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| Source note | uspto-grants-2016_07 |
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