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Nicotinic Acid → HCID 178418543, Verbindung

HRID 2380012
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2380012
C[C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][N:3]=1.C(O)(=[O:18])C1C=CC=NC=1.[Na].C(O)(=O)C1C=CC=NC=1>>[OH:18][C:4]1[N:3]=[CH:2][CH:10]=[CH:9][C:5]=1[C:6]([OH:8])=[O:7]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 938Nicotinic Acid2×HCID 1378606-Methylnicotinic acidHCID 66973663SODIUM NICOTINATE

Produkt 1

HCID 178418543HCID 178418543, VerbindungAusbeute 72,5 %

Versuchsvorschrift

The microorganisms with the designation Ki101 (DSM 6920) were incubated in 800 ml of mineral salt medium (Table 1 below) with addition of 8 mmol of 6-methylnicotinic acid in a 1 1 Fernbach flask at 30° C. on a shaker at 100 rpm. The inoculum was 5 percent (v/v). After 5 days, the OD650 was about 0.5. Then the cells were harvested and washed once with 50 m molar phosphate buffer, pH 7.0. Then the cells were resuspended in 20 ml of 50 mM of phosphate buffer, pH 7.0 containing 200 mg (1.38 mmol) of nicotinic acid-sodium salt. The OD650 was 20. After 6 hours incubation on a shaker at 30° C., no more nicotinic acid could be detected by thin-layer chromatography. Then the biomass was centrifuged off and the supernatant acidified to pH 2.5 to precipitate the 2-hydroxynicotinic acid. No contamination in the isolated product could be detected by 1H-NMR (DMSO) analysis. Altogether 140 mg (1 mmol) of 2-hydroxynicotinic acid corresponding to a yield of 72 percent relative to nicotinic acid could be isolated.

Aufarbeitung

  1. washwashed once with 50 m molar phosphate buffer, pH 7.0
  2. waitAfter 6 hours incubation on a shaker at 30° C.
  3. customto precipitate the 2-hydroxynicotinic acid

Quellen und Nachweise

ORD-Eintrag
ord-de85b44bb9f342038bfb89b5378da302
Quelldatensatz
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05364940

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