HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 493310Erstellt: 25. Oktober 2026
Ethylene carbonate → 2-(1,3-Benzoxazol-4-yloxy)ethanol
https://huagongshe.com/reaction/493310
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethylene carbonate | HCID 7303 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1,3-Benzoxazol-4-ol | HCID 13720697 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-(1,3-Benzoxazol-4-yloxy)ethanol | HCID 22036392 | — |
Reaktionsschritte
K2CO3 (254 mg, 1.84 mmol) was added to a stirred solution of 4-hydroxybenzoxazole* (248 mg, 1.84 mmol) in DMF (5 mL) at room temperature. The mixture was heated at 90° C. for 15 min and ethylene carbonate (176 mg, 2.00 mmol) was added. The mixture was stirred at 150° C. for 2 h and allowed to attain room temperature. The mixture was diluted with water (2 mL) and MeOH (2 mL), and concentrated. The residue was partitioned between water and CH2Cl2. The aqueous layer was separated and extracted with CH2Cl2 (2×10 mL). The organic phases were pooled and washed with water and brine, and dried over MgSO4. The filtrate was concentrated to give the product as a brown oil that slowly solidified: yield 278 mg (84%), mp 47-49° C. Anal (C9H9NO3) C, H, N.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07534794B2 |
|---|
| Quelldatensatz | uspto-grants-2009_05 |
|---|
| ORD ID | ord-cc74601e8b4f4fbdbb8e56bcc197d43c |
|---|
| Quellennotiz | uspto-grants-2009_05 |
|---|