反応 #2298668

ord-9b16f125bb8447fab0070e798ff49ac6

反応方程式

CC(=O)c1cc(Br)c(O)c(Br)c1
3,5-dibromo-4-hydroxyacetophenone
O=C([O-])[O-].[K+].[K+]
K2CO3
BrCCCBr
1,3- dibromopropane
CC(=O)c1cc(Br)c(OCCCBr)c(Br)c1
1-[4-(3-bromopropoxy)-3,5- dibromophenyl]ethanone

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度was heated
  2. 2
    温度at reflux for 5 hr
  3. 3
    その他The solvent was removed
  4. 4
    抽出The crude product was extracted into dichloromethane (150 ml)
  5. 5
    ろ過the insoluble inorganics were filtered off
  6. 6
    濃縮The solution was concentrated to dryness again
  7. 7
    その他Purification
  8. 8
    その他The material thus obtained (2.8 g)
  9. 9
    その他was recrystallized twice from isopropyl ether

実験手順

A stirred mixture of 3,5-dibromo-4-hydroxyacetophenone (3.0 g, 10.1 mmole), K2CO3 (2.8 g, 20.3 mmoles), 1,3- dibromopropane (4.0 g, 19.8 moles) in acetnotrile (100 ml) was heated at reflux for 5 hr. The solvent was removed. The crude product was extracted into dichloromethane (150 ml) and the insoluble inorganics were filtered off. The solution was concentrated to dryness again. Purification was carried out by flash chromatography on silica gel (45 g, SiO2; eluted with 1:1 hexane:dichloromethane). The material thus obtained (2.8 g) was recrystallized twice from isopropyl ether to give analytically pure 1-[4-(3-bromopropoxy)-3,5- dibromophenyl]ethanone, m.p.=87°-88° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE039265E1uspto-grants-2006_09