HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043791Generated: October 25, 2026
Diethyl fluoromalonate → HCID 178517898, compound
https://huagongshe.com/reaction/1043791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl fluoromalonate | HCID 12702 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Morpholine-4-carboximidamide Hydrobromide | HCID 2806564 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178517898 | HCID 178517898 | 12.6% |
Reaction Steps
Sodium hydride (60% in oil, 3.9 g, 96.5 mmol) was washed with hexanes in a round bottom flask under argon and cooled with an ice water bath. EtOH (100 mL) was slowly added. The resulting mixture was warmed to RT and stirred for 30 minutes. To the base mixture, diethyl 2-fluoromalonate (5.7 g, 32.2 mmol) was added, followed by morpholinoformamidine hydrobromide (6.8 g, 32.2 mmol). The mixture was heated to 90-95° C. with stirring under argon. After 12 hours, the reaction was cooled to room temperature and the EtOH was removed in vacuo. The resulting white solid was dissolved in water (25 mL) and acidified with conc. HCl to pH=3-4. A white precipitate formed which was collected on a Büchner filter, washed with water (2×50 mL), air dried on the filter, and dried in vacuo to give 5-fluoro-2-morpholinopyrimidine-4,6-diol (0.87 g, 12%). LC/MS (m/z): 216.0 (MH+), Rt 0.63 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08563549B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-92357aa0b697475ebba744cb2772c7e3 |
|---|
| Source note | uspto-grants-2013_10 |
|---|