Acetic Anhydride → Isosorbide-2-Acetate

HRID 1758094Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1758094
[C:1]([O:4][C:5](=[O:7])[CH3:6])(=O)[CH3:2].[CH2:8]1[O:12][C@@H:11]2[C@@H](O)C[O:15][C@@H:10]2[C@@H:9]1[OH:17].C([O-])(=O)C.[Na+]>C(O)(=O)C>[CH3:6][C:5]([O:4][C@@H:1]1[C@H:11]2[O:12][CH2:8][C@@H:9]([OH:17])[C@H:10]2[O:15][CH2:2]1)=[O:7]

Komponenten

5

Edukt 3

HCID 7918Acetic AnhydrideHCID 12597IsosorbideHCID 517045Sodium Acetate2×

Produkt 1

HCID 10856233Isosorbide-2-Acetate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

At approx. 100° C., 102 g (1 mol) of acetic acid anhydride are added to 146 g (1 mol) of isosorbide and 1 g of sodium acetate. This mixture is heated for half an hour under reflux and the acetic acid formed is then removed under a water-pump vacuum up to a sump temperature of approx. 140° C. An analysis of the residue shows that isosorbide, isosorbide-2-acetate, isosorbide-5-acetate and isosorbide-2,5-diacetate are present in approximately equal proportions. By the following transacylation and distillation, according to example 1, 182 g of raw isosorbide-2-acetate are obtained. After recrystallizing from 200 ml of acetone 92 g of pure isosorbide-2-acetate with a M.P. of 80° C. are obtained. The residue (90 g) remaining after concentrating the filtrate is again subjected to transacylation after adding 0.5 g of sodium acetate whereby again an almost quantitative yield of raw isosorbide-2-acetate is achieved. From this, 43 g of pure isosorbide-2-acetate and 46 g residue are obtained as described above. By another distillation in the presence of sodium acetate it is possible to prepare from the 46 g residue, 44 g of raw isosorbide-2-acetate from which, by recrystallisation, 26 g of pure isosorbide-2-acetate can be isolated. In this way a total amount of 161 g of pure isosorbide-2-acetate is obtained corresponding to 83% of the theory and 18 g residue which may be used for further transacylations. By repeating the above mentioned procedure resp. by adding the remaining residue to the next acylation batch an almost quantitative yield of pure isosorbide-2-acetate can be obtained.

Aufarbeitung

  1. temperatureThis mixture is heated for half an hour
  2. temperatureunder reflux
  3. customis then removed under a water-pump vacuum up to a sump temperature of approx. 140° C
  4. distillationBy the following transacylation and distillation
  5. customare obtained
  6. customAfter recrystallizing from 200 ml of acetone 92 g of pure isosorbide-2-acetate with a M.P. of 80° C.
  7. customare obtained
  8. concentrationafter concentrating the filtrate

Quellen und Nachweise

ORD-Eintrag
ord-f8c1b2508baf4c77910119b5ec9bb6b2
Quelldatensatz
uspto-grants-1983_02
Patentnummer
US04371703

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