Bromide ion → Isosorbide

HRID 848685Notes

Reaction equation

HRID 848685 reaction equation
[CH2:1]1[O:5][C@@H:4]2[C@@H:6]([OH:9])[CH2:7][O:8][C@@H:3]2[C@@H:2]1[OH:10].[Cl-].[Br-].[N+:13]([O-])([OH:15])=[O:14]>C(OC(=O)C)(=O)C>[CH2:1]1[O:5][C@@H:4]2[C@H:6]([O:9][N+:13]([O-:15])=[O:14])[CH2:7][O:8][C@@H:3]2[C@H:2]1[OH:10].[CH2:1]1[O:5][C@@H:4]2[C@@H:6]([OH:9])[CH2:7][O:8][C@@H:3]2[C@@H:2]1[OH:10]

Participants

7

Procedure

Finally, German published patent application No. P 27 51 934 and the corresponding U.S. Pat. No. 4,065,488 describe a process wherein isosorbide in a first step is esterified by reaction with a lower alkanoic anhydride, chloride or bromide, in particular acetic acid anhydride, to yield a mixture of isosorbide, isosorbide-2-acrylate, isosorbide-5-acylate and isosorbide-2.5-diacylate. In a second step, isosorbide is extracted from this mixture in order to avoid formation of isosorbide-2.5-dinitrate in the following nitration reaction which is dangerous as explosive. In a third step, the mixture of isosorbide-2-acylate, isosorbide-5-acylate and isosorbide-2.5-diacylate is subjected to nitration with nitric acid and the resulting mixture of isosorbide-2-acylate-5-nitrate, isosorbide-5-acylate-2-nitrate and isosorbide-2.5-diacylate is subjected to partial saponification resulting in a mixture of isosorbide-2-nitrate, isosorbide-5-nitrate and isosorbide. Isosorbide-5-nitrate finally is separated from this mixture by recrystallization from appropriate solvents. Thus, this process also is characterized by a multitude of reaction steps and has the further disadvantage that isosorbide contained in the mixture obtained in the first reaction step, has to be extracted in order to avoid the formation of the explosive isosorbide-2.5-dinitrate in the subsequent nitration reaction.

Workup

  1. customto yield
  2. extractionIn a second step, isosorbide is extracted from this mixture in order
  3. custom5-dinitrate in the following nitration reaction which

Sources & evidence

ORD record
ord-315d9a9dd82045029fa24a21eedcbc3c
Source dataset
uspto-grants-1981_10
Patent number
US04297286

Reaction notes

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