反応 #1121716

ord-87ba805f1ada4c0cb0c7fe7447ad93d2

反応方程式

Oc1ccc(O)cc1
hydroquinone
BrCCCCCCBr
1,6-dibromo hexane
[K+].[OH-]
Potassium hydroxide
Oc1ccc(OCCCCCCBr)cc1
4-(6-bromohexyloxy)phenol
収率 39.4%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他fluxed at 60° C.
  2. 2
    その他(Celsius) overnight
  3. 3
    その他is lowered to a room temperature
  4. 4
    その他methanol was evaporated from the reaction mixture
  5. 5
    抽出Then, the reaction mixture was extracted three times with water (100 ml (milliliters)) and ethyl acetate (100 ml (milliliters))
  6. 6
    その他Water was removed over magnesium sulfate
  7. 7
    その他the solvents were evaporated
  8. 8
    その他the resulting reaction mixture
  9. 9
    その他was purified

実験手順

As shown in the following Scheme, hydroquinone (1) (4.5 g (grams)) and 1,6-dibromo hexane (2) (10 g (grams)) were dissolved in methanol (100 ml (milliliters)) at a room temperature. Potassium hydroxide (2.3 g (grams)) was added to the resulting mixture solution, and then fluxed at 60° C. (Celsius) overnight. Next day, the temperature of the reaction mixture is lowered to a room temperature, and methanol was evaporated from the reaction mixture. Then, the reaction mixture was extracted three times with water (100 ml (milliliters)) and ethyl acetate (100 ml (milliliters)). Water was removed over magnesium sulfate, and the solvents were evaporated, and the resulting reaction mixture was purified using a column chromatography (developer solution: ethylacetate/hexane=1/5 volume ratio) to obtain 4.4 g (grams) of 4-(6-bromohexyloxy)phenol (3).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08545717B2uspto-grants-2013_10