HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6429Erstellt: 23. Oktober 2026
2-Aminophenol → 2-(2H-Pyrrol-2-ylidene)-2,3-dihydro-1,3-benzoxazole
https://huagongshe.com/de/reaction/6429
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Aminophenol | HCID 5801 | — |
| Edukt | Boric Acid | HCID 7628 | — |
| Edukt | Pyrrole-2-Carboxylic Acid | HCID 12473 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-(2H-Pyrrol-2-ylidene)-2,3-dihydro-1,3-benzoxazole | HCID 135625482 | 52% |
Reaktionsschritte
2-(Pyrrol-2-yl)benzoxazole was prepared as follows: A mixture of 5.55 g (0.05 mol) of pyrrole-2-carboxylic acid and 5.46 g (0.05 mol) of o-aminophenol and 3.09 g (0.05 mol) boric acid in 50 mL of xylene was heated under reflux for 3 days while removing water which was generated from reaction using a Dean-Stark trap. The cooled reaction mixture was diluted with 100 mL of ethyl acetate, washed with 150 mL of 5% sodium hydroxide solution and then with 150 mL of water. The separated organic layer was dried over anhydrous sodium sulfate. The resulting crude product was purified by column chromatography on silica gel with 20% hexane in chloroform as eluant. The desired product, 2-(pyrrol-2-yl)benzoxazole (4.75 g, 52%), was obtained as a white solid. m.p. 149°-150° C.; 1H NMR (CDCl3) δ6.38-6.40 (m, 1H, ArH), 7.05-7.06 (m, 1H, ArH), 7.11-7.13 (m, 1H, ArH), 7.29-7.36 (m, 2H, 2xArH), 7.53-7.56 (m, 1H, ArH), 7.65-7.69 (m, 1H, ArH), 10.9 (bs, 1H, NH).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05248782 |
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| Quelldatensatz | uspto-grants-1993_09 |
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| ORD ID | ord-2288569fc3ee4fffb9e3876b2052db84 |
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| Quellennotiz | uspto-grants-1993_09 |
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