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5-Chloro-2-phenylpyridine → 5-Ethyl-2-phenylpyridine

HRID 713558
ノート
印刷プレビュー

反応式

HRID 713558 の反応式
Cl[C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[N:6][CH:7]=1.[CH2:14]([Mg]Br)[CH3:15]>C1COCC1>[CH2:14]([C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[N:6][CH:7]=1)[CH3:15]
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

4

反応物 2

HCID 27628665-Chloro-2-phenylpyridineHCID 178418443HCID 178418443、化合物

生成物 1

HCID 5978535-Ethyl-2-phenylpyridine収率 19%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

5-Chloro-2-phenylpyridine (16 g, 84 mmol) and Ni(dppe)Cl2 (0.891 g, 1.687 mmol) were added to 300 mL of THF and the reaction mixture was degassed with nitrogen for 20 min. before being cooled to 0° C. Ethylmagnesium bromide (169 mL, 169 mmol) was added dropwise over a period of 60 min. and the reaction mixture stirred for and additional 3 h at before warming to room temperature overnight. The reaction mixture was recooled to 0° C. and quenched with 250 mL of water, extracted with EtOAc and the organic layer dried over sodium sulfate and filtered. The crude material was chromatographed on silica with 95/5 hexane/EtOAc to give 2.9 g (19%) of 5-ethyl-2-phenylpyridine as a white solid.

後処理

  1. customthe reaction mixture was degassed with nitrogen for 20 min.
  2. temperaturebefore warming to room temperature overnight
  3. customwas recooled to 0° C.
  4. customquenched with 250 mL of water
  5. extractionextracted with EtOAc
  6. dry with materialthe organic layer dried over sodium sulfate
  7. filtrationfiltered
  8. customThe crude material was chromatographed on silica with 95/5 hexane/EtOAc

出典と根拠

ORDレコード
ord-501eb203d6c542168dea71438a871f8d
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09184397B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート