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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminophenolHCID 5801—
EduktBoric AcidHCID 7628—
EduktPyrrole-2-Carboxylic AcidHCID 12473—
LösungsmittelO-XyleneHCID 7237—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(2H-Pyrrol-2-ylidene)-2,3-dihydro-1,3-benzoxazoleHCID 13562548252%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05248782
Quelldatensatzuspto-grants-1993_09
ORD IDord-2288569fc3ee4fffb9e3876b2052db84
Quellennotizuspto-grants-1993_09