Sucrose → HCID 11105894, Verbindung

HRID 854758

Reaktionsgleichung

Reaktionsgleichung von HRID 854758
C(O)[C@H]1O[C@H](O[C@]2(CO)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O.[CH3:24][O:25][C:26]([C:28]1[CH2:29][S:30][CH2:31][CH2:32][C:33]=1[OH:34])=[O:27]>O>[CH3:24][O:25][C:26]([C@H:28]1[C@@H:33]([OH:34])[CH2:32][CH2:31][S:30][CH2:29]1)=[O:27]

Komponenten

4

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

A suspension of baker's yeast (Saf-Instant yeast, 30 g) in water (700 mL) was treated with sucrose (142 g). The mixture was stirred at 25° C. for 6 h. At this time, 4-hydroxy-5,6-dihydro-2H-thiopyran-3-carboxylic acid methyl ester (4.06 g, 23.31 mmol) was added. The resulting slurry was stirred at 25° C. for 22 h and then was filtered through a pad of celite. The filtrate was extracted with ethyl acetate (5×300 mL). The combined organic extracts were washed with a saturated aqueous sodium chloride solution (1×150 mL), dried over magnesium sulfate, filtered, and concentrated in vacuo. Biotage chromatography (FLASH 40M, Silica, 3/1 hexanes/ethyl acetate) afforded 4(S)-hydroxy-tetrahydro-thiopyran-3(R)-carboxylic acid methyl ester (4.08 g, 99.3%) as a colorless oil: [α]23589=+37.76° (c=2.9, methanol)

Aufarbeitung

  1. stirringThe resulting slurry was stirred at 25° C. for 22 h
  2. filtrationwas filtered through a pad of celite
  3. extractionThe filtrate was extracted with ethyl acetate (5×300 mL)
  4. washThe combined organic extracts were washed with a saturated aqueous sodium chloride solution (1×150 mL)
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-9468fc0c879b464f9128a6c59bd72142
Quelldatensatz
uspto-grants-2007_08
Patentnummer
US07259166B2

Verknüpfte Notizen

Wird geladen…