반응식
C([O:3][C:4](=O)[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([Br:11])[CH:6]=1)C.O.[NH2:14][NH2:15]>C(O)C>[Br:11][C:7]1[CH:6]=[C:5]([CH:10]=[CH:9][CH:8]=1)[C:4]([NH:14][NH2:15])=[O:3]참가 물질
4
실험 절차
After 10 grams (44 mmol) of ethyl-3-bromobenzoate were placed into a 200 mL, three-neck flask, 50 mL of ethanol was added thereto and the mixture was stirred; 12 mL of hydrazine monohydrate was added, this mixture was stirred at 78° C. for 5 hours, and the contents of the flask were reacted together. After the reaction was completed, a solid was precipitated out with the addition of water to the reaction solution. The precipitate solid was removed by suction filtration. With the suction-filtered solid being placed into approximately 500 mL of water and washed and a solid removed by suction filtration, 8.1 grams of a white-colored solid, which was the objective of the synthesis process, were obtained at a yield of 86%.
후처리
- additionwas added
- stirringthis mixture was stirred at 78° C. for 5 hours
- customthe contents of the flask were reacted together
- customa solid was precipitated out with the addition of water to the reaction solution
- customThe precipitate solid was removed by suction filtration
- washwashed
- customa solid removed by suction filtration, 8.1 grams of a white-colored solid, which
- customwere obtained at a yield of 86%
출처 및 근거
- ORD 기록
- ord-c3be112600ce4a58aee544efac0496bb
- 출처 데이터셋
- uspto-grants-2012_07
- 특허 번호
- US08221904B2
연결된 노트
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