반응식
[C:1]([Br:5])(Br)(Br)Br.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.OC[C:27]1[O:31][N:30]=[C:29]([C:32]([O:34][CH2:35][CH3:36])=[O:33])[CH:28]=1>C1COCC1>[Br:5][CH2:1][C:27]1[O:31][N:30]=[C:29]([C:32]([O:34][CH2:35][CH3:36])=[O:33])[CH:28]=1참가 물질
5
실험 절차
Carbon tetrabromide (5.44 g; 16.39 mmol) was added to the solution of triphenylphosphine (4.34 g, 16.39 mmol) in THF (50 mL) and the resulting mixture was stirred at room temperature for 15 min. To this green suspension was added a solution of ethyl 5-(hydroxymethyl)isoxazole-3-carboxylate (1.87 g, 10.93 mmol) in THF (10 mL) and the resulting reaction mixture was stirred overnight at room temperature. The solid material was removed by filtration. The filtrate was concentrated under reduced pressure and the residue was purified by flash chromatography on silica gel (eluent: 15 to 100% dichloromethane in heptane) to afford 1.73 g (68%) of ethyl 5-(bromomethyl)isoxazole-3-carboxylate as a solid.
후처리
- customthe resulting reaction mixture
- stirringwas stirred overnight at room temperature
- customThe solid material was removed by filtration
- concentrationThe filtrate was concentrated under reduced pressure
- customthe residue was purified by flash chromatography on silica gel (eluent: 15 to 100% dichloromethane in heptane)
출처 및 근거
- ORD 기록
- ord-3bdb08645a304d71abee182697af6870
- 출처 데이터셋
- uspto-grants-2016_09
- 특허 번호
- US09434722B2
연결된 노트
불러오는 중…