Water → 2-(3-Hydroxypropyl)-2-phenyl-1,3-dioxolane
Reaction equation
C1[O:17][C:4](OC)([CH2:5][CH2:6][C:7](=[O:14])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)OC1.[H-].[H-].[H-].[H-].[Li+].[Al+3].O.[OH-].[K+].C1C[O:30][CH2:29][CH2:28]1>>[CH2:28]1[O:14][C:7]([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)([CH2:6][CH2:5][CH2:4][OH:17])[O:30][CH2:29]1Participants
Procedure
A solution of methyl 3-benzoylpropionate ethylene ketal (7.9661 g, 33.7 mmol), prepared in the previous step in 150 ml of anhydrous THF was added under nitrogen dropwise over 1 hour to a suspension of LAH (1.6656 g, 43.9 mmol) in 75 ml of anhydrous THF. After the addition the mixture was stirred at room temperature for 19 hours. Water (1.7 ml) was then added dropwise followed by the addition of 1.7 ml of 15% KOH and then 5.1 ml of water. The resulting mixture was stirred for 15 minutes and then filtered. The filtrate was concentrated under reduced pressure to remove most of the THF. The residue was partitioned between methylene chloride-water. The organic layer was separated and the aqueous layer extracted two times with methylene chloride. The combined organic extracts were dried (MgSO4) and the solvent removed under reduced pressure to give 4-hydroxybutyrophenone ethylene ketal (6.51 g, 93%) as a white solid, mp 39-42° C.
Workup
- additionAfter the addition the mixture
- stirringThe resulting mixture was stirred for 15 minutes
- filtrationfiltered
- concentrationThe filtrate was concentrated under reduced pressure
- customto remove most of the THF
- customThe residue was partitioned between methylene chloride-water
- customThe organic layer was separated
- extractionthe aqueous layer extracted two times with methylene chloride
- dry with materialThe combined organic extracts were dried (MgSO4)
- customthe solvent removed under reduced pressure
Sources & evidence
- ORD record
- ord-555d9f70bd00448eb8871e62124a2aa0
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05977170
Reaction notes
Loading…