Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Palmitoyl chloride | HCID 8206 | — |
| Reactant | N-Acetyl-D-Glucosamine | HCID 439174 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69270369 | HCID 69270369 | — |
Reaction Steps
To 1 g of N-acetylglucosamine, 5 mL of pyridine and 15 mL of N,N-dimethylformamide were added, and the mixture was heated to 70° C. under stirring and 1.37 mL of palmitoyl chloride was dropwise added, and the reaction was carried out for 4 hours. On completion of the reaction, after extracting with ethyl acetate and washing with 2 mol/L hydrochloric acid, the ethyl acetate layer was dried over anhydrous magnesium sulfate and then the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent; chloroform:methanol=15:1) to obtain 710 mg of 2-acetamido-2-deoxy-6-O-palmitoyl-α-D-glucopyranose as a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07393937B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-ca9b18613cc2481cbec58b30dec84c68 |
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| Source note | uspto-grants-2008_07 |
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