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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279926Erstellt: 25. Oktober 2026

Acetic Acid → 1,2-diamino-1,2-dideoxy-D-glucitol

https://huagongshe.com/reaction/279926

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktPhenylhydrazineHCID 7516—
EduktSodium BicarbonateHCID 516892—
Edukt(3R,4R,5S,6R)-3-amino-6-(hydroxymethyl)oxane-2,4,5-triol hydrochlorideHCID 2723635—
KatalysatorDipotassium tetrachloroplatinateHCID 61440—
LösungsmittelWaterHCID 962—
Produkt1,2-diamino-1,2-dideoxy-D-glucitolHCID 13631651—

Reaktionsbedingungen

Temperatur4 °C

Reaktionsschritte

A solution of 20 g of glucosamine hydrochloride, 20 ml of glacial acetic acid, 80 ml of water and 9.1 ml of phenylhydrazine was heated on a steam bath for one hour, then cooled and filtered. The filtrate was hydrogenated in a Parr apparatus with Raney nickel catalyst until the uptake of hydrogen ceased. This mixture was then filtered, the filtrate was treated with activated charcoal and refiltered through diatomaceous earth, giving a green solution. A 6.31 ml portion of this green solution was treated with 0.24 g of sodium bicarbonate and a suspension of 1.66 g of potassium tetrachloroplatinate in 8 ml of water. The resulting reddish brown solution was stirred overnight, then cooled to 4° C. for 3 hours and the resulting solid collected. A 100 mg portion of this solid was stirred with 15 ml of hot water and then filtered through diatomaceous earth. The filtrate was cooled giving a solid which was collected, giving 90 mg of 1,2-diamino-1,2-dideoxy-D-glucitol, compound with platinum chloride (1:1) as yellow grains, mp 265° C. (dec.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04587331
Quelldatensatzuspto-grants-1986_05
ORD IDord-0dd8cedb2cb44f4cb56ff4b974d81c4e
Quellennotizuspto-grants-1986_05