Potassium Carbonate → HCID 54478685, compound

HRID 1631864Notes

Reaction equation

HRID 1631864 reaction equation
Br[CH2:2][CH2:3][C:4]([O:6][CH2:7][CH2:8][O:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][C:17]([C:20]([C:22]([OH:40])([CH2:24][C:25]2[CH:30]=[CH:29][C:28]([O:31][CH2:32][CH2:33][O:34][C:35](=[O:39])[CH2:36][CH2:37]Br)=[CH:27][CH:26]=2)[CH3:23])=[O:21])([OH:19])[CH3:18])=[CH:12][CH:11]=1)=[O:5].C([O-])([O-])=O.[K+].[K+]>CC(C)=O>[C:4]([O:6][CH2:7][CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]([CH2:16][C:17]([C:20]([C:22]([OH:40])([CH2:24][C:25]2[CH:30]=[CH:29][C:28]([O:31][CH2:32][CH2:33][O:34][C:35](=[O:39])[CH:36]=[CH2:37])=[CH:27][CH:26]=2)[CH3:23])=[O:21])([OH:19])[CH3:18])=[CH:14][CH:15]=1)(=[O:5])[CH:3]=[CH2:2]

Participants

4

Procedure

5.2 g (14.5 mmol) 4-(2-(3-bromopropionyloxy)ethoxy)phenyl-2-hydroxy-2-propyl ketone was dissolved in 45 ml acetone. 30 mg BHT and 3.0 g (21.75 mmol) K2CO3 were added and the reaction mixture was refluxed for 5 hours. The reaction mixture was allowed to cool down to room temperature and the inorganic salts were removed by filtration. The solvent was removed under reduced pressure and the residue was treated with 50 ml n.-hexane. 4-(2-acryloyloxyethoxy)phenyl-2-hydroxy-2-propyl ketone was isolated by filtration. 3 g of 4-(2-acryloyloxyethoxy)phenyl-2-hydroxy-2-propyl ketone (75%) was isolated as a white crystalline compound.

Workup

  1. temperaturethe reaction mixture was refluxed for 5 hours
  2. customthe inorganic salts were removed by filtration
  3. customThe solvent was removed under reduced pressure
  4. additionthe residue was treated with 50 ml n

Sources & evidence

ORD record
ord-6dcd0553a20a47ef9a81e6bcceece3cb
Source dataset
uspto-grants-2014_07
Patent number
US08791289B2

Reaction notes

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