Resorcinol → 1,8-Bis(3-Hydroxyphenoxy)Octane

HRID 5537

反応式

HRID 5537 の反応式
[C:1]1([CH:8]=[CH:7][CH:6]=[C:4]([OH:5])[CH:3]=1)[OH:2].Br[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17]Br.[OH-:19].[K+]>O>[OH:2][C:1]1[CH:3]=[C:4]([CH:6]=[CH:7][CH:8]=1)[O:5][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][O:19][C:4]1[CH:6]=[CH:7][CH:8]=[C:1]([OH:2])[CH:3]=1

参加物

5

反応条件

温度
10 °C

実験手順

A five neck five liter round bottom flask equipped with a mechanical stirrer, two condensers, and a dropping funnel is purged with nitrogen then charged under a nitrogen blanket with 1.6 kg (14.5 moles) resorcinol, 160 grams deionized water, and 296.7 grams (1.091 moles) 1,8-dibromooctane. The easily stirable reaction mass is slowly heated to reflux under a slow nitrogen purge. A solution of 181 grams (2.74 moles) 85% KOH pellets in 184 grams water is added dropwise at reflux under a nitrogen blanket over a period of two hours. After about 25% of the KOH has been added, the reaction mass has dissolved to light tea colored solution then it becomes increasingly clouded as salt is formed. The reaction mixture is refluxed an additional hour after all the KOH has been added. The pH of the reaction mixture is basic. The reaction is quenched with 1.5 liters of water and acidified with 40% sulfuric acid. The reaction mixtures is then poured into 4 liters of water, cooled in an ice bath to a temperature of 10° C. and filtered to recover a tan colored solid which is slurried in 1.2 liters boiling water to wash out resorcinol and KBr. The cooled slurry is then filtered and 350 grams of crude product is recovered. Crystallization from 400 ml acetone yield 170 grams white crystals, 88% pure by HPLC peak area, and recrystallization from 500 ml acetone yields 97.4 grams product of 96% purity by HPLC peak area and high purity by gel permeation chromatography (m.p. 78°-82° C.).

後処理

  1. customA five neck five liter round bottom flask equipped with a mechanical stirrer
  2. customtwo condensers, and a dropping funnel is purged with nitrogen
  3. temperatureThe easily stirable reaction mass is slowly heated
  4. temperatureto reflux under a slow nitrogen
  5. custompurge
  6. temperatureat reflux under a nitrogen blanket over a period of two hours
  7. dissolutionthe reaction mass has dissolved to light tea colored solution
  8. temperatureit becomes increasingly clouded as salt
  9. customis formed
  10. additionhas been added
  11. customThe reaction is quenched with 1.5 liters of water
  12. customThe reaction mixtures
  13. filtrationfiltered
  14. customto recover a tan colored solid which
  15. washto wash out resorcinol and KBr
  16. filtrationThe cooled slurry is then filtered
  17. custom350 grams of crude product is recovered
  18. customCrystallization from 400 ml acetone yield 170 grams white crystals, 88%
  19. custompure by HPLC peak area, and recrystallization from 500 ml acetone

出典と根拠

ORDレコード
ord-d7ebeb5510864bf5a76d01a064162923
出典データセット
uspto-grants-1993_09
特許番号
US05244998

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