Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 387473생성일: 2026년 10월 26일
4-Hydroxybenzoic acid hydrazide → 4-[5-(3-Chloro-phenylamino)-[1,3,4]oxadiazol-2-yl]-phenol
https://huagongshe.com/reaction/387473
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Hydroxybenzoic acid hydrazide | HCID 1742 | — |
| 반응물 | 3-Chlorophenyl isothiocyanate | HCID 75449 | — |
| 촉매 | Mercuric oxide | HCID 30856 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 4-[5-(3-Chloro-phenylamino)-[1,3,4]oxadiazol-2-yl]-phenol | HCID 136179696 | 89.7% |
반응 단계
Mercury (II) oxide yellow (6.38 g, 29.47 mmol) was suspended in ca. 100 mL of anhydrous methanol. 4-Hydroxybenzoic acid hydrazide (4.48 g, 29.47 mmol) was added to this bright-orange suspension, followed by 3-chlorophenylisothiocyanate (5.0 g, 29.47 mmol). The reaction mixture was brought to reflux and refluxed for 2 hours. The reaction mixture turned pitch-black in color and formed black precipitate. Then it was cooled down to ambient temperature and filtered through a short pad of Celite. Then it was purified by silica gel chromatography using 0% to 20% methanol gradient in EtOAc. Solvent was removed in vacuo and the resulting grey precipitate was re-crystallized from ca. 50 mL of EtOAc. The formed white crystalline solid was filtered, washed with a small amount of EtOAc, anhydrous Et2O and dried in vacuo to give the title product as a white powder (7.606 g). Yield 89.7%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08372971B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-b6e4b48d93c546c19fd9d73a427b8ecf |
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| 출처 메모 | uspto-grants-2013_02 |
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