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Diethyl Ether → Ethyl 2-(2-bromopyrimidin-5-yl)acetate

HRID 546881
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HRID 546881 반응식
[Br:1][Si](C)(C)C.[CH2:6]([O:8][C:9](=[O:18])[CH2:10][C:11]1[CH:12]=[N:13][C:14](Cl)=[N:15][CH:16]=1)[CH3:7].C(OCC)C.[OH-].[Na+]>C(#N)CC>[CH2:6]([O:8][C:9](=[O:18])[CH2:10][C:11]1[CH:12]=[N:13][C:14]([Br:1])=[N:15][CH:16]=1)[CH3:7]
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6

반응물 4

HCID 3283Diethyl EtherHCID 14798Sodium HydroxideHCID 76113BromotrimethylsilaneHCID 57443497Ethyl 2-(2-chloropyrimidin-5-yl)acetate

생성물 1

HCID 57443494Ethyl 2-(2-bromopyrimidin-5-yl)acetate수율 91%

시약·촉매·용매 1

HCID 7854Propionitrile용매

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온도
101.5 °C

실험 절차

Bromotrimethylsilane (1.7 mL, 12 mmol) was added to a solution of (2-chloro-pyrimidin-5-yl)acetic acid ethyl ester (Example 43-(2); 810 mg, 4.04 mmol) in propionitrile (4 mL), and the mixture was heated under reflux at an external temperature of 98 to 105° C. for nine hours. After cooling the reaction mixture to room temperature, diethyl ether was added to the reaction mixture, which was neutralized with a 2 N sodium hydroxide aqueous solution (6.3 mL). The reaction mixture was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel chromatography (hexane/ethyl acetate=2/1) to give the title compound (897 mg, 91%).

후처리

  1. temperaturethe mixture was heated
  2. temperatureAfter cooling the reaction mixture to room temperature
  3. extractionThe reaction mixture was extracted with diethyl ether
  4. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel chromatography (hexane/ethyl acetate=2/1)

출처 및 근거

ORD 기록
ord-2e2011b630ac49d9a214f5afece34942
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07935688B2

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