HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2300040Erstellt: 26. Oktober 2026
Pyridine → 1,3-Dibenzyl-5-(phenylacetyl)barbituric acid
https://huagongshe.com/reaction/2300040
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Phenylacetyl chloride | HCID 7679 | — |
| Edukt | Mls002704122 | HCID 268729 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1,3-Dibenzyl-5-(phenylacetyl)barbituric acid | HCID 9954190 | 88,8% |
Reaktionsschritte
To a solution of 1,3-dibenzyl barbituric acid 192 mg (0.623 mmol) in dry dichloromethane 2.0 mL under nitrogen atmosphere, added was pyridine 1.0 mL (12 mmol) and stirred at 0° C. Added was phenylacetyl chloride 96 mg (0.623 mmol, 1.00 equivalent) in dichloromethane 1.0 mL to the solution slowly during a period of 20 minutes, then stirred at room temperature for 3 hours. Added was dichloromethane 40 mL and washed the organic layer with 2 M hydrochloric acid and saturated brine, and dried over sodium sulfate. Purified was the crude product 273 mg, after removal of the solvent under the reduced pressure, by column chromatography (silica gel, eluted with dichloromethane). It obtained 1,3-dibenzyl-5-(phenylacetyl)barbituric acid 236 mg as colorless viscous oil at first (88.7% yield) and it gradually turned white plates.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06498164B1 |
|---|
| Quelldatensatz | uspto-grants-2002_12 |
|---|
| ORD ID | ord-dabb582cc5aa4dabb93a2cbe0caa81d9 |
|---|
| Quellennotiz | uspto-grants-2002_12 |
|---|