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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564893Generated: October 27, 2026

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

https://huagongshe.com/reaction/564893

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 0.1 M 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 numberUS06168934A
Source datasetuspto-grants-2001_01
ORD IDord-10e5b3c2258c483fbb9f17af566e4737
Source noteuspto-grants-2001_01