1-(4-((3,4-Dichlorobenzyl)oxy)phenyl)ethanone → 2-Bromo-1-[4-(3,4-dichloro-benzyloxy)-phenyl]-ethanone
반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:16]=[CH:17][C:18]=1[Cl:19])[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([C:13](=[O:15])[CH3:14])=[CH:9][CH:8]=1.C1CNC(=O)C1.[Br:26][Br-]Br>CO.C(Cl)Cl>[Br:26][CH2:14][C:13]([C:10]1[CH:9]=[CH:8][C:7]([O:6][CH2:5][C:4]2[CH:16]=[CH:17][C:18]([Cl:19])=[C:2]([Cl:1])[CH:3]=2)=[CH:12][CH:11]=1)=[O:15]참가 물질
실험 절차
1-[4-(3,4-Dichloro-benzyloxy)-phenyl]-ethanone (2.92 g) was dissolved in methanol:DCM (2:1, 75 mL) and pyrrolidinone hydrotribromide (7.5 g) was added and stirred at room temperature for 2.5 h. After completion of the reaction, the mixture was concentrated in vacuo and poured into saturated sodium bicarbonate solution (100 mL) and extracted with ethyl acetate (2×100 mL). The organic extracts were combined and concentrated in vacuo. Then this residue was dissolved in DCM (10 ml) and methanol (10 mL) was slowly added to this solution to precipitate the product. The colored solution was filtered through to give clear white powder product 2-bromo-1-[4-(3,4-dichloro-benzyloxy)-phenyl]-ethanone with quantitative yield (3.75 g). 1H NMR (400 MHz, CDCl3): 7.98 (d, 2H), 7.54 (s, 1H), 7.47 (d, 1H), 7.25 (m, 1H), 7.01 (d, 2H), 5.09 (s, 2H), and 4.40 (s, 2H).
후처리
- customAfter completion of the reaction
- concentrationthe mixture was concentrated in vacuo
- additionpoured into saturated sodium bicarbonate solution (100 mL)
- extractionextracted with ethyl acetate (2×100 mL)
- concentrationconcentrated in vacuo
- dissolutionThen this residue was dissolved in DCM (10 ml)
- additionmethanol (10 mL) was slowly added to this solution
- customto precipitate the product
- filtrationThe colored solution was filtered through
출처 및 근거
- ORD 기록
- ord-299d119364d54fb4be9dcfb4bb86b4ed
- 출처 데이터셋
- uspto-grants-2013_02
- 특허 번호
- US08383644B2
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