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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051672Generated: October 30, 2026

Sodium Acetate → 4-O-Acetyl-1,5-anhydro-2,3,6-trideoxy-3-[(2,2,2-trifluoro-1-hydroxyethylidene)amino]hex-1-enitol

https://huagongshe.com/reaction/2051672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantHCID 54522117HCID 54522117—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product4-O-Acetyl-1,5-anhydro-2,3,6-trideoxy-3-[(2,2,2-trifluoro-1-hydroxyethylidene)amino]hex-1-enitolHCID 19450977%

Reaction Steps

To a mixture of 18 g. of zinc dust and 1.8 g. of cupric sulfate in 60 ml. of 50% aqueous acetic acid containing 25 g. of sodium acetate, 10 g. of the product of Examples 10 and 11 in 10 ml. of acetic acid is added dropwise at -10° C. The reaction is continued for 4 hours at -10° C., after which the zinc dust and copper are removed by filtration, 50 g. of ice is added to the filtrate, and the filtrate is extracted three times with chloroform. The combined extracts are washed with water, a cold saturated sodium hydrogen carbonate solution, and water. After the chloroform solution is dried over anhydrous magnesium sulfate, it is evaporated in vacuo to a heavy syrup. The syrupy residue is crystallized from a mixture of ether-petroleum ether to give 4.7 g. (77% yield) of 3-trifluoroacetamido-4-O-acetyl-1,2,3,6-tetradeoxy-L-lyxo-hex-1-enepyranose.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04181795
Source datasetuspto-grants-1980_01
ORD IDord-72585f0e34164afaa3e3992a028f2fe7
Source noteuspto-grants-1980_01