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

HRID 1746024
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HRID 1746024 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-9f1da921f36d4e47a7d9e2469f6690fd
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE045720E1

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