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L-Fucal → 1,5-anhydro-3-oxo-2,3,6-trideoxy-L-threo-hex-1-enitol

HRID 1155326
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1155326
[CH3:1][C@@H:2]1[O:7][CH:6]=[CH:5][C@H:4]([OH:8])[C@@H:3]1[OH:9]>C1C=CC=CC=1.C(=O)([O-])[O-].[Ag+2].C([O-])([O-])=O.[Ag+].[Ag+]>[O:8]=[C:4]1[C@H:3]([OH:9])[C@H:2]([CH3:1])[O:7][CH:6]=[CH:5]1
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Komponenten

5

Edukt 1

HCID 11083911L-Fucal

Produkt 1

HCID 128167791,5-anhydro-3-oxo-2,3,6-trideoxy-L-threo-hex-1-enitol

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 92796Silver carbonateKatalysatorHCID 178418647HCID 178418647, VerbindungKatalysatorHCID 241BenzeneLösungsmittel

Versuchsvorschrift

In a 250 milliliter round-bottomed flask, 1 gram of L-fucal [Example 5 product] is dissolved in 100 milliliters of benzene. To this solution was added 20-25 grams of silver carbonate on celite (Fetizon's reagent), prepared as described below, and the mixture was stirred. The flask was equipped for simple distillation, and 20-25 milliliters of solvent was removed by distillation. During this time the yellow Fetizon's reagent becomes dark brown. The distillation assembly is replaced with an efficient reflux condenser and the mixture is refluxed for 1 hour, after which time the reaction is generally completed as judged by t.l.c. monitoring. The hot mixture is filtered through celite and the filtrate evaporated under reduced pressure to give 1,5-anhydro-3-oxo-2,3,6-trideoxy-L-threo-hex-1-enitol.

Aufarbeitung

  1. customprepared
  2. customwas removed by distillation
  3. distillationThe distillation
  4. customassembly is replaced with an efficient reflux condenser
  5. temperaturethe mixture is refluxed for 1 hour
  6. filtrationThe hot mixture is filtered through celite
  7. customthe filtrate evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-166bebeb578e4543948968928c145247
Quelldatensatz
uspto-grants-1981_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04301276

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