Hydrogen Bromide → 1-(1-Bromoethyl)-3-nitrobenzene
반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10](O)[CH3:11])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[BrH:13]>C(O)(=O)C.C(Cl)Cl>[Br:13][CH:10]([C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=1)[CH3:11]참가 물질
5
실험 절차
26.15 g (156 mmol) of 1-(3-nitrophenyl)ethanol are dissolved in 130 ml of glacial acetic acid, and 55 ml (313 mmol) of 33% HBr in glacial acetic acid are added dropwise with ice cooling. The reaction mixture is stirred at room temperature for 5 days. The mixture is subsequently diluted with 300 ml of DCM, washed with 3×200 ml of H2O and 200 ml of saturated NaHCO3 solution, dried over sodium sulfate and evaporated to dryness, and the residue is crystallised from petroleum ether.
후처리
- washwashed with 3×200 ml of H2O and 200 ml of saturated NaHCO3 solution
- dry with materialdried over sodium sulfate
- customevaporated to dryness
- customthe residue is crystallised from petroleum ether
출처 및 근거
- ORD 기록
- ord-26e5f94bbbb64bf9adb31032db0c486d
- 출처 데이터셋
- uspto-grants-2013_04
- 특허 번호
- US08431572B2
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