Water → 4-Bromo-1-[(2,2-dimethoxyethyl)oxy]-2-methylbenzene
반응식
[CH3:1][O:2][CH:3]([O:6][CH3:7])[CH2:4]Br.[Br:8][C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[C:11]([CH3:16])[CH:10]=1.[OH-].[K+].O>CS(C)=O>[Br:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH2:4][CH:3]([O:6][CH3:7])[O:2][CH3:1])=[C:11]([CH3:16])[CH:10]=1참가 물질
반응 조건
- 온도
- 100 °C
실험 절차
Bromoacetaldehyde dimethylacetal (6.05 ml) was added to a stirred solution of 4-bromo-2-methylphenol (10.0 g) and KOH (5.0 g) in dry DMSO (40 ml). The solution was warmed to 100° C. for 4 hours. After this time the reaction mixture was cooled to room temperature and poured into water (200 ml). The aqueous layer was extracted with ether (2×100 ml). The combined organic layers were separated, washed with 2N aqueous NaOH (2×50 ml), dried over MgSO4, filtered, and the solvent removed under reduced pressure to afford a brown oil. Purification by MPLC (15% ethyl acetate/n-hexane) afforded 4-bromo-1-[(2,2-dimethoxyethyl)oxy]-2-methylbenzene as a colourless oil (6.24 g). 1H NMR (360 MHz,CDCl3)δ2.21 (3H, s), 3.46 (6H,s), 3.98 (2H, d, J=3.6 Hz), 4.69 (1H, t, J=3.6 Hz), 6.56 (1H, d, J=7.2 Hz), 7.26 (1H, d, J=7.2 Hz), 7.39 (1H, s).
후처리
- temperatureAfter this time the reaction mixture was cooled to room temperature
- extractionThe aqueous layer was extracted with ether (2×100 ml)
- customThe combined organic layers were separated
- washwashed with 2N aqueous NaOH (2×50 ml)
- dry with materialdried over MgSO4
- filtrationfiltered
- customthe solvent removed under reduced pressure
- customto afford a brown oil
- customPurification by MPLC (15% ethyl acetate/n-hexane)
출처 및 근거
- ORD 기록
- ord-e78fc456644a4f88bab3628c5d1a01b8
- 출처 데이터셋
- uspto-grants-1999_11
- 특허 번호
- US05985896
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