참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Aminophenol | HCID 5801 | — |
| 반응물 | Boric Acid | HCID 7628 | — |
| 반응물 | Pyrrole-2-Carboxylic Acid | HCID 12473 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-(2H-Pyrrol-2-ylidene)-2,3-dihydro-1,3-benzoxazole | HCID 135625482 | 52% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05248782 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-2288569fc3ee4fffb9e3876b2052db84 |
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| 출처 메모 | uspto-grants-1993_09 |
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