Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-Acetyl-D-Mannosamine | HCID 439281 | — |
| Edukt | 3-Butenoic acid, ion(1-) | HCID 6971089 | — |
| Edukt | Ethylacetate methanol | HCID 21584119 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | GlyTouCan:G94857MO | HCID 14160859 | 92% |
Reaktionsschritte
In 2 mL of DMF were suspended 500 mg (2.2 mmol) of N-acetylmannosamine. Vinylacetate (1 mL, 5 equivalent) and 160 mg of subtilisin mutant 8399 [Zhong et al., J. Am. Chem. Soc., 113:683 (1991)] were then added and the suspension was stirred vigorously at room temperature. The reaction progress was monitored by TLC with ethyl acetate/methanol (2/1). After 5 hours when the formation of the di-acetylated derivatives began, the reaction was stopped by evaporating the vinylacetate and DMF. Methanol was then added to dissolve the sugar. After the enzyme and salt were filtered off, the filtrate was concentrated. The residual syrup was chromatographed on a silica gel, with ethyl acetate/methanol (10/1) to give 6-O-Acetyl N-acetylmannosamine (92 percent) as α/β mixture (3:1) based on the NMR spectrum.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05759823 |
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| Quelldatensatz | uspto-grants-1998_06 |
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| ORD ID | ord-a1e01a17b76e4861aa30b7110edb48ad |
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| Quellennotiz | uspto-grants-1998_06 |
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