HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → N-Benzoyl-3-phenylisoserine, (2R,3S)-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Benzoyl chloride | HCID 7412 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 3-Phenylisoserine, (2R,3S)- | HCID 7020763 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-Benzoyl-3-phenylisoserine, (2R,3S)- | HCID 2762289 | 72% |
Reaktionsschritte
To a solution of compound 5.HCl (219 mg, 1.00 mmol) in water (10 mL) containing sodium bicarbonate (500 mg, 5.95 mmol) was added a solution of benzoyl chloride (0.14 mL, 1.20 mmol) in dichloromethane (5.0 mL). The mixture was vigorously stirred for 16 h at room temperature. The reaction mixture was acidified with 0.1N HCl and the crude product was extracted with ethyl acetate (40 mL×3). The combined organic extracts were dried over anhydrous magnesium sulfate and concentrated in vacuo to dryness. The residue was purified on a short silica gel column using chloroform/methanol (2/1) as the eluant to give N-benzoyl-(2R,3S)-3-phenylisoserine (6) (205 mg, 72%) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05294737 |
| Quelldatensatz | uspto-grants-1994_03 |
| ORD ID | ord-01d7f9b6a7c348acb29c19cf0c535ecb |
| Quellennotiz | uspto-grants-1994_03 |