反応 #1178396

ord-3172d48492684866a26c03fcf649f011

反応方程式

Cl
HCl
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCNCC
diethyl amine
BrCc1ccc(Br)cc1
p-bromobenzyl bromide
CCN(CC)Cc1ccc(Br)cc1
(p-bromobenzyl)diethyl amine
収率 74.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONwas added
  2. 2
    抽出The mixture was extracted with 100 ml diethyl ether for three times
  3. 3
    乾燥The diethyl ether solution was dried with anhydrous magnesium sulfate over night
  4. 4
    その他the magnesium sulfate was removed by filtration
  5. 5
    その他Diethyl ether was evaporated
  6. 6
    その他the raw product was purified by a silica gel column

実験手順

Into a 500 ml round-bottomed flask were added 150 ml THF, 5 ml water, 2.2 g potassium carbonate, 6 ml diethyl amine, and 5 g p-bromobenzyl bromide. The resultant mixture was refluxed for 12 h. The mixture was then cooled to room temperature, into which 6 ml concentrated HCl was added, followed by the addition of 150 ml water. The mixture was extracted with 100 ml diethyl ether for three times. The diethyl ether solution was dried with anhydrous magnesium sulfate over night and then the magnesium sulfate was removed by filtration. Diethyl ether was evaporated and the raw product was purified by a silica gel column using hexane/chloroform mixture (1:1 by volume) as the eluent. (p-bromobenzyl)diethyl amine (BBDA) was obtained in 74% yield (3.6 g).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08129111B2uspto-grants-2012_03