Benzyl Alcohol → HCID 18594626, compound
Reaction equation
[C:1]([O:4][C@@H:5]([CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH2:6][CH2:7][C@@H:8]1[C@@H:12]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]([O:21][CH3:22])=[O:20])[C:11](=[O:23])[CH2:10][CH2:9]1)(=[O:3])[CH3:2].[C:29]1([CH3:39])[CH:34]=[CH:33][C:32](S(O)(=O)=O)=[CH:31][CH:30]=1.[CH2:40]([OH:47])[C:41]1[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=1>>[C:1]([O:4][C@@H:5]([CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH2:6][CH2:7][C@@H:8]1[C@@H:12]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]([O:21][CH3:22])=[O:20])[C:11]([O:47][CH2:40][C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=2)([O:23][CH2:39][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH2:10][CH2:9]1)(=[O:3])[CH3:2]Participants
4
Procedure
A solution of 2 g. of l-methyl 15(S)-acetoxy-9-oxo prostanoate (Example 52) and 25 mg. of p-toluene sulfonic acid in 65 ml. of benzylalcohol is stirred at 100° C. for 6 hours. The solution is concentrated to near dryness under reduced pressure. The residue is diluted with ether and the resulting solution is washed with 5% sodium carbonate solution, saturated sodium chloride solution, dried with anhydrous sodium sulfate and taken to dryness to afford 2.5 g. of product.
Workup
- concentrationThe solution is concentrated
- additionThe residue is diluted with ether
- washthe resulting solution is washed with 5% sodium carbonate solution, saturated sodium chloride solution
- dry with materialdried with anhydrous sodium sulfate
- customto afford 2.5 g
Sources & evidence
- ORD record
- ord-30a940bd41154e4da1d1b0b557db01e5
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04017534
Reaction notes
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