Water → 1-(2-Bromoethoxy)-4-iodobenzene

HRID 1007835ノート

反応式

HRID 1007835 の反応式
[I:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.C([O-])([O-])=O.[K+].[K+].[Br:15][CH2:16][CH2:17]Br.O>CN(C=O)C>[Br:15][CH2:16][CH2:17][O:8][C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][CH:4]=1

参加物

6

反応条件

温度
50 °C

実験手順

To a stirring solution of 4-iodophenol (25 g, 110 mmol) and K2CO3 (31 g, 220 mmol) in DMF (250 mL) was added 1,2-dibromoethane (5 mL, 55 mmol) over a period of 1 hr. The solution was heated at 50° C. and stirred overnight under Ar. In order to complete the reaction additional reagents were added: 1,2-dibromoethane (20 mL, 220 mmol) and K2CO3 (6 g, 43 mmol) and the mixture was heated at 50° C. an additional 12 hours under Ar. Water was added and the reaction mixture was extracted with dichloromethane, dried over Na2SO4, filtered and the solvent evaporated under reduced pressure. The crude mixture was purified by silica gel chromatography eluted with 10% ethyl acetate in hexanes to give the title compound as a white solid (5.5 g, 17 mmol).

後処理

  1. additionwere added
  2. extractionthe reaction mixture was extracted with dichloromethane
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. customthe solvent evaporated under reduced pressure
  6. customThe crude mixture was purified by silica gel chromatography
  7. washeluted with 10% ethyl acetate in hexanes

出典と根拠

ORDレコード
ord-902abd28bd764115be4b5c2aafc56df3
出典データセット
uspto-grants-2004_09
特許番号
US06797713B2

反応ノート

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