Hydrochloric Acid → 1-(6-Chloropyrimidin-4-yl)ethan-1-one
반응식
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([O:10]CC)=[CH2:9])[N:5]=[CH:4][N:3]=1.Cl>CC(C)=O>[Cl:1][C:2]1[N:3]=[CH:4][N:5]=[C:6]([C:8](=[O:10])[CH3:9])[CH:7]=1참가 물질
4
실험 절차
4-Chloro-6-[1-(ethyloxy)ethenyl]pyrimidine (Intermediate 17, 3.54 g, 19.17 mmol) was dissolved in acetone (177 mL), treated with 2M aqueous hydrochloric acid solution (28.8 mL, 57.5 mmol) and the resulting mixture was stirred at room temperature for 18 hours. The solvent was removed under reduced pressure. The residue was neutralised with aqueous saturated sodium bicarbonate solution and extracted with ethyl acetate (×2). The ethyl acetate layers were combined, dried under magnesium sulfate and evaporated under reduced pressure to give the title compound as a white solid (2.30 g);
후처리
- customThe solvent was removed under reduced pressure
- extractionextracted with ethyl acetate (×2)
- customdried under magnesium sulfate
- customevaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-a7553d8829d3406b8e834eeafe3f7f94
- 출처 데이터셋
- uspto-grants-2014_08
- 특허 번호
- US08796283B2
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