Benzene → 24-Hydroxyvitamin D2

HRID 481285Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 481285
[CH3:1][CH:2]([C@:4]([OH:30])(/[CH:6]=[CH:7]/[C@H:8]([C@@H:10]1[C@:27]2([CH3:28])[C@H:13]([C:14]3[C@H:24]([CH2:25][CH2:26]2)[C@:22]2([CH3:23])[C:17]([CH2:18][C@@H:19]([OH:29])[CH2:20][CH2:21]2)=[CH:16][CH:15]=3)[CH2:12][CH2:11]1)[CH3:9])[CH3:5])[CH3:3].C1C=CC=CC=1.O>CCOCC>[CH3:9][C@@H:8]([C@@H:10]1[C@@:27]2([CH3:28])[CH2:26][CH2:25][CH2:24]/[C:14](=[CH:15]\[CH:16]=[C:17]3\[CH2:18][C@@H:19]([OH:29])[CH2:20][CH2:21][C:22]\3=[CH2:23])/[C@@H:13]2[CH2:12][CH2:11]1)/[CH:7]=[CH:6]/[C:4]([OH:30])([CH:2]([CH3:1])[CH3:3])[CH3:5]

Komponenten

5

Versuchsvorschrift

One gram (2.4 mmol) of (7) was dissolved in 250 ml of ether and benzene (4:1) and irradiated with stirring under nitrogen in a water-cooled quartz immersion well using a Hanovia medium-pressure UV lamp for 2 hrs. The solution was concentrated in vacuo, redissolved in 100 ml of ethanol and heated under reflux overnight. The solution was concentrated to dryness in vacuo and the residue was purified on a silica gel column using 30% ethyl acetate in hexane to yield 0.55 g (55%) of (8).

Aufarbeitung

  1. customfor 2 hrs
  2. concentrationThe solution was concentrated in vacuo
  3. dissolutionredissolved in 100 ml of ethanol
  4. temperatureheated
  5. temperatureunder reflux overnight
  6. concentrationThe solution was concentrated to dryness in vacuo
  7. customthe residue was purified on a silica gel column

Quellen und Nachweise

ORD-Eintrag
ord-78103c7c16f84491beed458cf3b9a084
Quelldatensatz
uspto-grants-1998_08
Patentnummer
US05789397

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