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Cesium carbonate → 5-Bromo-2-chloro-3-(4-propoxybenzyl)thiophene

HRID 1469176
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HRID 1469176 반응식
[Br:1][C:2]1[S:6][C:5]([Cl:7])=[C:4]([CH2:8][C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=2)[CH:3]=1.I[CH2:17][CH2:18][CH3:19].C([O-])([O-])=O.[Cs+].[Cs+]>CC(C)=O>[Br:1][C:2]1[S:6][C:5]([Cl:7])=[C:4]([CH2:8][C:9]2[CH:14]=[CH:13][C:12]([O:15][CH2:17][CH2:18][CH3:19])=[CH:11][CH:10]=2)[CH:3]=1
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참가 물질

5

반응물 3

HCID 10796Cesium carbonateHCID 336431-IodopropaneHCID 666909044-((5-Bromo-2-chlorothiophen-3-yl)methyl)phenol

생성물 1

HCID 666936375-Bromo-2-chloro-3-(4-propoxybenzyl)thiophene수율 105.2%

시약·촉매·용매 1

HCID 180Acetone용매

반응 조건

온도
60 °C

실험 절차

To a solution of phenol 4 (500 mg, 1.65 mmol) in acetone (25 mL) were added 1-iodopropane (0.5 mL, 4.95 mmol) and Cs2CO3 (460 mg, 4.95 mmol) at room temperature. The mixture was stirred at 60° C. for 12 hours. The reaction mixture was cooled to room temperature and filtered off through celite. The filtrate was concentrated in vacuo. The residue was purified by silica column chromatography (Biotage) to provide the title compound 5 (600 mg, 99%).

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. filtrationfiltered off through celite
  3. concentrationThe filtrate was concentrated in vacuo
  4. customThe residue was purified by silica column chromatography (Biotage)

출처 및 근거

ORD 기록
ord-958801c9981e4be9b26bf2dc402475e9
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09006187B2

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