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Triethylamine → 5-Bromo-2-(4-fluoro-phenoxymethyl)-pyridine

HRID 77993
ノート
印刷プレビュー

反応式

HRID 77993 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[H-].[Na+].Cl.[Br:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:19]Cl)=[N:17][CH:18]=1.C(N(CC)CC)C>C(OCC)(=O)C.O.CN(C)C=O>[Br:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:19][O:8][C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=2)=[N:17][CH:18]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 8471TriethylamineHCID 97324-FluorophenolHCID 24758Sodium hydrideHCID 534382005-Bromo-2-(chloromethyl)pyridine hydrochloride

生成物 1

HCID 592552365-Bromo-2-(4-fluoro-phenoxymethyl)-pyridine収率 63.6%

試薬・触媒・溶媒 3

HCID 962Water溶媒
HCID 6228
Dimethylformamide
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

To an N,N-dimethylformamide (40.0 mL) solution of 4-fluorophenol (3.00 g, 26.8 mmol) was added sodium hydride (1.00 g, 25.0 mmol, 60% in oil) on an ice bath (0° C.) under nitrogen atmosphere, which was stirred for 20 minutes at room temperature. To the reaction solution was then added a mixture of 5-bromo-2-chloromethyl-pyridine hydrochloride (4.6 g, 22.3 mmol) described in Manufacturing Example 54-1-2 and triethylamine (30.6 mL, 20.4 mmol), which was stirred for 10 minutes at room temperature. Water and ethyl acetate were added to the reaction mixture, and the organic layer was extracted with ethyl acetate. This organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The solvent was evaporated from the filtrate under a reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:4) to obtain the title compound (4.0 g, 63.6%).

後処理

  1. additionTo the reaction solution was then added
  2. stirringwas stirred for 10 minutes at room temperature
  3. extractionthe organic layer was extracted with ethyl acetate
  4. washThis organic layer was washed with water and saturated aqueous sodium chloride
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customThe solvent was evaporated from the filtrate under a reduced pressure
  8. customthe residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:4)

出典と根拠

ORDレコード
ord-7c71563111e545da838ab2302ab4d6a1
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08841327B2

反応ノート

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