Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
5-(2-nitrophenyl)-3H-1,3,4-oxadiazol-2-one → 5-(2-Aminophenyl)-1,3,4-oxadiazol-2(3H)-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 5-(2-nitrophenyl)-3H-1,3,4-oxadiazol-2-one | HCID 312921 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 5-(2-Aminophenyl)-1,3,4-oxadiazol-2(3H)-one | HCID 12858148 | 93.1% |
반응 단계
A solution of 2-nitrobenzoylhydrazine (9.05 g, 0.05 mol) in dioxane (30 mL) was slowly added to a solution of trichloromethyl chloroformate (4.6 mL, 0.04 mol) in dioxane (30 mL) at room temperature. On completion of the addition the reaction was heated to reflux for 4 hours. The solvent was evaporated off and the residue re-crystallised from 96%. ethanol (50 mL) to give 7.15 g of the 5-(2-nitrophenyl)-3H-[1,3,4]oxadiazol -2-one. M.p. 157-158° C. A solution of the nitro compound (2 g, 9.7 mmol) in 96% ethanol (25 mL) was hydrogenated over 5% palladium on charcoal to give desired 1.6 g of the desired amine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06297261B1 |
| 출처 데이터셋 | uspto-grants-2001_10 |
| ORD ID | ord-f78aa3592ecc4746adebbabc51b8c5ee |
| 출처 메모 | uspto-grants-2001_10 |