Benzyl Alcohol → HCID 18594626, compound

HRID 328520Notes

Reaction equation

HRID 328520 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

  1. concentrationThe solution is concentrated
  2. additionThe residue is diluted with ether
  3. washthe resulting solution is washed with 5% sodium carbonate solution, saturated sodium chloride solution
  4. dry with materialdried with anhydrous sodium sulfate
  5. 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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