2-Chloroethanol → 2-tert-Butyl-4-(2-hydroxyethoxy)phenol

HRID 1885907ノート

反応式

HRID 1885907 の反応式
[C:1]([C:5]1[CH:11]=[C:10]([OH:12])[CH:9]=[CH:8][C:6]=1[OH:7])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+].[CH2:15](Cl)[CH2:16][OH:17].S(=O)(=O)(O)O>O.[I-].[K+]>[C:1]([C:5]1[CH:11]=[C:10]([O:12][CH2:15][CH2:16][OH:17])[CH:9]=[CH:8][C:6]=1[OH:7])([CH3:4])([CH3:2])[CH3:3]

参加物

7

反応条件

温度
80 °C

実験手順

332 g (2 mol) of t-butylhydroquinone and 1 g of potassium iodide were dissolved in 2 l of water under nitrogen atmosphere, and were heated to 80° C. Thereafter, to the solution thus obtained, were dropwise added 232 g (2.8 mol) of 48% sodium hydroxide aqueous solution and 200 g (2.5 mol) of ethylene chlorohydrine at the same time for 3 hours while constantly maintaining alkaline. After finishing this dropwise addition, the resultant reaction mixture was heated for 8 hours at the reflux temperature. After cooling the reaction mixture thus obtained, the reaction mixture was neutralized with sulfuric acid and was extracted with toluene. After removing solvent, the remaining material was distilled under reduced pressure and the distillate was recrystallized from toluene to obtain 200 g of 2-t-butyl-4-(2'-hydroxyethoxy)phenol. The reaction formula (alkylation) is illustrated in the following. ##STR4##

後処理

  1. customThereafter, to the solution thus obtained
  2. customfor 3 hours
  3. temperaturewhile constantly maintaining alkaline
  4. additionthis dropwise addition
  5. customthe resultant reaction mixture
  6. temperaturewas heated for 8 hours at the reflux temperature
  7. temperatureAfter cooling the reaction mixture
  8. customthus obtained
  9. extractionwas extracted with toluene
  10. customAfter removing solvent
  11. distillationthe remaining material was distilled under reduced pressure
  12. customthe distillate was recrystallized from toluene

出典と根拠

ORDレコード
ord-f0fcf766ae6b4a88877865bba3043c1b
出典データセット
uspto-grants-1992_09
特許番号
US05147902

反応ノート

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