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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233548Generated: October 25, 2026

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

https://huagongshe.com/reaction/233548

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, 0.5M 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 numberUS05593887
Source datasetuspto-grants-1997_01
ORD IDord-741cf5ac689a4803a5cf3c18601112e1
Source noteuspto-grants-1997_01