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tert-Butyldimethylsilyl chloride → 2-(t-Butyldimethylsilyl)-3-bromo-4-methoxy benzaldehyde

HRID 131092
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HRID 131092 반응식
O[C:2]1[C:9]([Br:10])=[C:8]([O:11][CH3:12])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[Si:13](Cl)([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14]>CN(C=O)C>[Si:13]([C:2]1[C:9]([Br:10])=[C:8]([O:11][CH3:12])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5])([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14]
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참가 물질

4

반응물 2

HCID 28928tert-Butyldimethylsilyl chlorideHCID 141209453-Bromo-2-hydroxy-4-methoxybenzaldehyde

생성물 1

HCID 223492562-(t-Butyldimethylsilyl)-3-bromo-4-methoxy benzaldehyde수율 83.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Diiospropylethylamine (3.0 ml) was added to a stirred solution (under argon) of 2-hydroxy-3-bromo- -4-methoxybenzaldehyde (1.96, 8.5 mmole) in DMF (15 ml) followed by t-butyldimethlsilyl chloride (TBSCl, 1.91 g, 12.8 mmole). The reaction mixture was stirred at room temperature for 30 min and Ice (20 g) was added to the mixture. The mixture was then extracted with ether (3×25 ml). The ethereal solution was washed with water (25 ml) and saturated NaHCO3 solution (2×15 ml). The solvent evaporated to yield 2-(t-butyldimethylsilyl)-3-bromo-4-methoxy benzaldehyde as an oil (2.54 g, 7.06 mmole, 83.1%).

후처리

  1. extractionThe mixture was then extracted with ether (3×25 ml)
  2. washThe ethereal solution was washed with water (25 ml) and saturated NaHCO3 solution (2×15 ml)
  3. customThe solvent evaporated

출처 및 근거

ORD 기록
ord-705325ef04a849a39f8f6379eeb183ef
출처 데이터셋
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07384925B2

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