Pyridine → 3-(2-Ethoxyphenoxy)-1,2-propanediol

HRID 1613357

反応式

HRID 1613357 の反応式
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10])[CH3:2].[CH2:11]1[O:13][CH:12]1[CH2:14][OH:15].N1C=CC=CC=1>C(O)C>[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[O:10][CH2:11][CH:12]([OH:13])[CH2:14][OH:15])[CH3:2]

参加物

5

反応物 3

HCID 1049PyridineHCID 11164GlycidolHCID 667552-Ethoxyphenol

生成物 1

HCID 688253-(2-Ethoxyphenoxy)-1,2-propanediol収率 65.6%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A solution of 41.5 g (0.3 mole) of 2-ethoxyphenol, 29.6 g (0.4 mole) of glycidol, 2 ml of pyridine and 150 ml of absolute ethanol was heated at reflux temperature for 18 hr. The mixture was concentrated to a thick oil that crystallized slowly over several days. The crude product was chromatographed on a silica gel column (1.2 kg) using increasing portions of acetone in methylene chloride to elute the product. The desired fractions were combined and concentrated to give a yellow oil that crystallized on standing. The solid was triturated with petroleum ether and the mixture filtered to obtain 41.8 g of solid. Recrystallization from carbon tetrachloride yielded 37.2 g (58%) of white solid, mp 64°-65° C.

後処理

  1. temperatureat reflux temperature for 18 hr
  2. concentrationThe mixture was concentrated to a thick oil that
  3. customcrystallized slowly over several days
  4. customThe crude product was chromatographed on a silica gel column (1.2 kg)
  5. temperatureusing increasing portions of acetone in methylene chloride
  6. washto elute the product
  7. concentrationconcentrated
  8. customto give a yellow oil that
  9. customcrystallized
  10. customThe solid was triturated with petroleum ether
  11. filtrationthe mixture filtered

出典と根拠

ORDレコード
ord-221ca49d55d6430fb84367ada06de27b
出典データセット
uspto-grants-1993_03
特許番号
US05192785

関連ノート

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