HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915899Generated: October 31, 2026
(E)-2,3-dibromo-4-oxobut-2-enoic acid → 5-Bromo-2-(2-fluorophenyl)pyrimidine-4-carboxylic acid
https://huagongshe.com/reaction/1915899
Participants
| Role | Name | HCID | Charge |
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| Reactant | (E)-2,3-dibromo-4-oxobut-2-enoic acid | HCID 2723705 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2-Fluorobenzamidine | HCID 4323059 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Bromo-2-(2-fluorophenyl)pyrimidine-4-carboxylic acid | HCID 82168673 | — |
Reaction Steps
Sodium ethoxide (21 mass % in ethanol; 8.69 mL, 23.268 mmol) was added to an ice-bath cooled mixture of 2-fluorobenzamidine (2.71 g, 15.512 mmol) in ethanol (100 mL). The resulting mixture was allowed to warm to room temperature and stirred at rt (room temperature) under nitrogen for 30 min. To the reaction mixture was added a solution of (E)-2,3-dibromo-4-oxo-but-2-enoic acid (2.00 g, 7.7561 mmol) in ethanol (20 ml). The mixture was heated at 50° C. for 3 h. After cooling to RT, the reaction was concentrated in vacuo. Water and 1M NaOH (˜50 ml) were added and the aqueous mixture was extracted with EtOAc. The aqueous phase was acidified to pH4 with 1N HCl (about 30 ml), then extracted with EtOAc 3×. Combined organic extracts were dried over sodium sulfate, filtered and concentrated to gave 5-bromo-2-(2-fluorophenyl)pyrimidine-4-carboxylic acid, 770 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614206B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-f66b542cb56249499a1599913708a013 |
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| Source note | uspto-grants-2013_12 |
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