Sulfuric acid magnesium salt (1:1) → HCID 20530959, compound
Reaction equation
[CH2:1]([O:8][CH:9]([CH2:30][CH2:31][CH2:32][CH2:33][CH3:34])[CH2:10][CH2:11][N:12]1[C:16](=[O:17])[CH:15](C(OCC)=O)[C:14](=[O:23])[CH:13]1[CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S([O-])([O-])(=O)=O.[Mg+2]>CCOCC>[CH2:1]([O:8][CH:9]([CH2:30][CH2:31][CH2:32][CH2:33][CH3:34])[CH2:10][CH2:11][N:12]1[C:16](=[O:17])[CH2:15][C:14](=[O:23])[CH:13]1[CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The solution of 1-(3'-benzyloxy-n-octyl)-4-ethoxycarbonyl-2-(ethoxycarbonylmethyl)-pyrrolidin-3,5-dione in ether (obtained as described above) was stirred overnight in the presence of magnesium sulphate. The mixture was filtered and the filtrate was evaporated in vacuo giving 1-(3'-benzyloxy-n-octyl)-2-(ethoxycarbonylmethyl)pyrrolidin-3,5-dione [71 g., 95% overall yield for steps b) and c)] as a yellow oil.
Workup
- filtrationThe mixture was filtered
- customthe filtrate was evaporated in vacuo
Sources & evidence
- ORD record
- ord-a96870f1d2a94fca9aa9715636ffe712
- Source dataset
- uspto-grants-1982_07
- Patent number
- US04341708
Reaction notes
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