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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211062Generated: October 27, 2026

Acrylamide → 5-N-Acetyl-9-O-acetyl-neuraminic acid

https://huagongshe.com/reaction/2211062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylamideHCID 6579—
ReactantN-Acetyl-Neuraminic AcidHCID 439197—
ReactantGlyTouCan:G81315WSHCID 131719162—
SolventWaterHCID 962—
SolventPotassium Phosphate, TribasicHCID 62657—
SolventPyruvateHCID 107735—
SolventD-1,4-DithiothreitolHCID 446094—
Product5-N-Acetyl-9-O-acetyl-neuraminic acidHCID 9204274447%

Reaction Steps

In a 10 mL of 0.1M potassium phosphate buffer (pH 7.5) were dissolved 10 mM DTT, 0.5 M pyruvate, 100 mg of 6-O-acetylmannosamine, prepared as described above, and 1.5 mg NeuAc aldolase (36 U). The reaction mixture was incubated at 37° C. for 8 days followed by lyophilization. The lyophilized powder was dissolved in a small amount of water and directly applied to a Bio Gel P-2 column (3×90 cm) and eluted with a flow rate of 6 mL/40 minutes at 4° C. To remove the trace amount of contaminated NeuAc due to the hydrolysis of the product, another gel filtration was required. Compound 201 was obtained in 47 percent yield. Its physical data were consistent with the reported data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05461143
Source datasetuspto-grants-1995_10
ORD IDord-5bbcbc1a5461403a8d0432d96f3fddb9
Source noteuspto-grants-1995_10