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HRID 6429作成日:2026年10月23日

2-Aminophenol → 2-(2H-Pyrrol-2-ylidene)-2,3-dihydro-1,3-benzoxazole

https://huagongshe.com/ja/reaction/6429

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminophenolHCID 5801—
反応物Boric AcidHCID 7628—
反応物Pyrrole-2-Carboxylic AcidHCID 12473—
溶媒O-XyleneHCID 7237—
溶媒Ethyl AcetateHCID 8857—
生成物2-(2H-Pyrrol-2-ylidene)-2,3-dihydro-1,3-benzoxazoleHCID 13562548252%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248782
出典データセットuspto-grants-1993_09
ORD IDord-2288569fc3ee4fffb9e3876b2052db84
出典メモuspto-grants-1993_09