Methanesulfonic Acid → HCID 23293363, compound

HRID 1599774Notes

Reaction equation

HRID 1599774 reaction equation
[CH3:1][C:2]([C:4]1[CH:5]=[CH:6][C:7](O)=[CH:8][CH:9]=1)=[O:3].CS(O)(=O)=[O:13].[O:16]1[CH:21]=[CH:20][CH2:19][CH2:18][CH2:17]1>C(OCC)(=O)C>[O:16]1[CH2:17][CH2:18][CH:19]([O:13][CH2:1][C:2]([C:4]2[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=2)=[O:3])[CH2:20][CH2:21]1

Participants

5

Procedure

4-Hydroxyacetophenone (75.00 g, 0.55 mol) was dissolved in ethyl acetate (300 ml) and a catalytic amount of methanesulfonic acid. The solution was cooled to 0°-4° C. Dihydropyran (204 ml, 2.20 moles, 4.0 eq) was slowly added. At the end of the addition, the ice-water bath was removed and the reaction was allowed to proceed at room temperature. A few minutes later a heavy white precipitate was formed and the slurry was transferred into a separatory funnel where it was washed with water. The organic layer was dried over anhydrous sodium sulfate. Removal of the solvent under reduced pressure afforded a white fluffy solid. The solid was recrystallized from hexane. The yield was quantitative.

Workup

  1. temperatureThe solution was cooled to 0°-4° C
  2. additionAt the end of the addition
  3. customthe ice-water bath was removed
  4. customto proceed at room temperature
  5. customA few minutes later a heavy white precipitate was formed
  6. customthe slurry was transferred into a separatory funnel
  7. washwhere it was washed with water
  8. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  9. customRemoval of the solvent under reduced pressure
  10. customafforded a white fluffy solid
  11. customThe solid was recrystallized from hexane

Sources & evidence

ORD record
ord-7135dec69007476aaf69a661fc267f7e
Source dataset
uspto-grants-1998_04
Patent number
US05741924

Reaction notes

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