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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 54522117 | HCID 54522117 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-O-Acetyl-1,5-anhydro-2,3,6-trideoxy-3-[(2,2,2-trifluoro-1-hydroxyethylidene)amino]hex-1-enitol | HCID 194509 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04181795 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-72585f0e34164afaa3e3992a028f2fe7 |
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| Source note | uspto-grants-1980_01 |
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