Water → HO(CH2)4OCH(CH3)CH2OCH2Ph

HRID 2182016Notes

Reaction equation

HRID 2182016 reaction equation
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][OH:6].[OH-].[K+].S(O[CH:20]([CH2:22][O:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[CH3:21])(C1C=CC(C)=CC=1)(=O)=O.O>O1CCOCC1>[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][O:6][CH:20]([CH2:22][O:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[CH3:21]

Participants

6

Conditions

Temperature
102 °C

Procedure

HO(CH2)4OH (37 g), potassium hydroxide (23 g) and dioxane (200 ml) were charged into a four necked flask and heated to an internal temperature of 102° C. to dissolve potassium hydroxide. A solution of TsOCH(CH3)CH2OCH2Ph (63.7 g) obtained in Example 2-1 in dioxane (65 ml), was dropwise added over a period of 1 hour and stirred for 4 hours. The mixture was left to cool, then added to water (350 ml) and extracted three times with dichloromethane (100 ml). The organic layer was washed with water (20 ml). It was dried over magnesium sulfate, filtered and then concentrated by an evaporator to obtain a crude product (52 g). It was purified by silica gel column chromatography to obtain the above-identified compound (27.6 g).

Workup

  1. waitThe mixture was left
  2. temperatureto cool
  3. extractionextracted three times with dichloromethane (100 ml)
  4. washThe organic layer was washed with water (20 ml)
  5. dry with materialIt was dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated by an evaporator
  8. customto obtain a crude product (52 g)
  9. customIt was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-ae9750acf03e4b33946c688544f05b19
Source dataset
uspto-grants-2005_05
Patent number
US06894187B2

Reaction notes

Loading…