HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 380098Erstellt: 26. Oktober 2026
Benzoin → (5R)-5-(4,5-diphenyloxazol-2-yl)pyrrolidin-2-one
https://huagongshe.com/reaction/380098
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzoin | HCID 8400 | — |
| Edukt | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Edukt | D-Pyroglutamic acid | HCID 439685 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (5R)-5-(4,5-diphenyloxazol-2-yl)pyrrolidin-2-one | HCID 54104002 | — |
Reaktionsschritte
To a solution of D-pyroglutamic acid (30 g) in CH2Cl2 (200 ml) were added benzoin (74 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (68 ml) and 4-dimethylaminopyridine (30 g) at room temperature under N2. After being stirred for 12 hours at room temperature, the solvent was evaporated in vacuo, and the residue was partitioned between ethyl acetate and water. The organic layer was washed with 1N-HCl solution, sat. NaHCO3 and brine, dried over MgSO4, and evaporated in vacuo. The obtained compound and ammonium acetate (60 g) were dissolved in acetic acid (500 ml) and the mixture was stirred for 4 hours at 100° C. After the solvent was removed, the residue was partitioned between ethyl acetate and water. The organic layer was washed with water, sat. NaHCO3 and brine. The dried solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel to give (5R)-5-(4,5-diphenyloxazol-2-yl)pyrrolidin-2-one (21.2 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06300344B1 |
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| Quelldatensatz | uspto-grants-2001_10 |
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| ORD ID | ord-4711f1f8d222417aacbc503ba9706a33 |
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| Quellennotiz | uspto-grants-2001_10 |
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