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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279926Generated: October 25, 2026

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

https://huagongshe.com/reaction/279926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPhenylhydrazineHCID 7516—
ReactantSodium BicarbonateHCID 516892—
Reactant(3R,4R,5S,6R)-3-amino-6-(hydroxymethyl)oxane-2,4,5-triol hydrochlorideHCID 2723635—
CatalystDipotassium tetrachloroplatinateHCID 61440—
SolventWaterHCID 962—
Product1,2-diamino-1,2-dideoxy-D-glucitolHCID 13631651—

Reaction Conditions

Temperature4 °C

Reaction Steps

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.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04587331
Source datasetuspto-grants-1986_05
ORD IDord-0dd8cedb2cb44f4cb56ff4b974d81c4e
Source noteuspto-grants-1986_05