Bromine → 2-(3-bromo-2-oxopropyl)-2,3-dihydro-1H-isoindole-1,3-dione
반응식
C1O[C:4]([CH2:6][N:7]2[C:11](=[O:12])[C:10]3=[CH:13][CH:14]=[CH:15][CH:16]=[C:9]3[C:8]2=[O:17])([CH3:5])[O:3]C1.[Br:19]Br>C(O)COCCO>[C:11]1(=[O:12])[N:7]([CH2:6][C:4](=[O:3])[CH2:5][Br:19])[C:8](=[O:17])[C:9]2=[CH:16][CH:15]=[CH:14][CH:13]=[C:10]12참가 물질
실험 절차
A solution of phthalimidoacetone ethylene ketal (2.47 g, 10 mmole) in 10 mlof diethylene glycol is heated on a steambath. To this hot solution bromine(1.6 g, 10 mmole) is added dropwise under nitrogen. The reaction mixture iscooled to room temperature and is quenched in 20 ml hexane. To this mixtureis added solid sodium carbonate followed by chloroform and ice water. The organic layer is separated and the aqueous layer is extracted 3 times withchloroform. The chloroform extracts are washed with water, dried over anhydrous sodium sulfate, and evaporated in vacuo. The residue is crystallized from ethyl acetate/hexane to afford 2 g (55%) of (3-phthalimidoacetonyl)bromide, ethylene ketal as white prisms of melting point 139°-141° C. An analytical sample has a melting point of 140°-141° C.
후처리
- customiscooled to room temperature
- customis quenched in 20 ml hexane
- additionTo this mixtureis added solid sodium carbonate
- customThe organic layer is separated
- extractionthe aqueous layer is extracted 3 times withchloroform
- washThe chloroform extracts are washed with water
- dry with materialdried over anhydrous sodium sulfate
- customevaporated in vacuo
- customThe residue is crystallized from ethyl acetate/hexane
출처 및 근거
- ORD 기록
- ord-e86698a3bae247f08e7b36a409820ba3
- 출처 데이터셋
- uspto-grants-1976_11
- 특허 번호
- US03992408
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