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1,2-Difluorobenzene → HCID 21477972、化合物

HRID 2374117
ノート
印刷プレビュー

反応式

HRID 2374117 の反応式
C([Li])CCC.[F:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[F:13].[CH:14](=[O:23])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22].[Cl-].[NH4+]>C1COCC1>[F:6][C:7]1[C:8]([F:13])=[CH:9][CH:10]=[CH:11][C:12]=1[CH:14]([OH:23])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]
参加物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 97061,2-DifluorobenzeneHCID 25517Ammonium ChlorideHCID 31289NonanalHCID 178418339Butyllithium

生成物 1

HCID 21477972HCID 21477972、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

Butyllithium (2.5 M in hexanes 52.5 ml, 0.131 mol) was added dropwise to a stirred, cooled (−78° C.) solution of difluorobenzene (12.0 g, 0.105 mol) in dry THF (400 ml) under a stream of dry nitrogen. The reaction mixture was maintained under these conditions for 2.5 h and a solution of nonanal (14.9 g, 0.105 mol) in dry THF (50 ml) was added dropwise at −78° C. The mixture was allowed to slowly reach room temperature overnight. Ammonium chloride solution (2M, 200 ml) was added and the product was extracted into ether (2×150 ml), the combined ethereal extracts were washed with water and dried (MgSO4). The solvent was removed in vacuo and the residue was distilled under reduced pressure to give a colourless oil.

後処理

  1. temperatureThe reaction mixture was maintained under these conditions for 2.5 h
  2. customwas allowed to slowly reach room temperature overnight
  3. extractionthe product was extracted into ether (2×150 ml)
  4. washthe combined ethereal extracts were washed with water
  5. dry with materialdried (MgSO4)
  6. customThe solvent was removed in vacuo
  7. distillationthe residue was distilled under reduced pressure
  8. customto give a colourless oil

出典と根拠

ORDレコード
ord-bea9daa0aa9c4e17911f833deb936290
出典データセット
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07462427B2

反応ノート

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