Acetic Anhydride → HCID 70603769, compound
Reaction equation
[OH:1][CH:2]([CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[CH:3]=[CH:4][C@@H:5]1[CH2:9][CH2:8][C:7](=[O:10])[C@H:6]1[CH2:11]/[CH:12]=[CH:13]\[CH2:14][CH2:15][CH2:16][C:17]([O:19][CH3:20])=[O:18].[C:26](OC(=O)C)(=[O:28])[CH3:27]>N1C=CC=CC=1>[C:26]([O:1][CH:2]([CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[CH:3]=[CH:4][C@@H:5]1[CH2:9][CH2:8][C:7](=[O:10])[C@H:6]1[CH2:11]/[CH:12]=[CH:13]\[CH2:14][CH2:15][CH2:16][C:17]([O:19][CH3:20])=[O:18])(=[O:28])[CH3:27]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of the compound of formula I, methyl trans,cis-7-[2-(3-hydroxy-1-octenyl)-5-oxocyclopentyl]-5-heptenoate (5 g), described in Example 161, in 50 ml of pyridine and 50 ml of acetic anhydride is stirred at room temperature for 4 hr. The solution is diluted with ice-water and extracted with ether. The ether is washed with 10% H2SO4, water 10% Na2CO3 and water, dried (Na2SO4) and evaporated to give the title compound.
Workup
- extractionextracted with ether
- washThe ether is washed with 10% H2SO4, water 10% Na2CO3 and water
- dry with materialdried (Na2SO4)
- customevaporated
Sources & evidence
- ORD record
- ord-abd3c628b5e94807b60355df1260519d
- Source dataset
- uspto-grants-1978_07
- Patent number
- US04100343
Reaction notes
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