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

HRID 546881
ノート
印刷プレビュー

反応式

HRID 546881 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 7854Propionitrile溶媒

反応条件

温度
101.5 °C

実験手順

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%).

後処理

  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)

出典と根拠

ORDレコード
ord-2e2011b630ac49d9a214f5afece34942
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07935688B2

反応ノート

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