Reaktionsgleichung
C(O)C.[CH3:4][C@@H:5]([C@@H:13]1[C@@:17]2([CH3:33])[CH2:18][CH2:19][CH2:20]/[C:21](=[CH:22]\[CH:23]=[C:24]3\[CH2:25][C@@H:26]([OH:32])[CH2:27][C@H:28](O)[C:29]\3=[CH2:30])/[C@@H:16]2[CH2:15][CH2:14]1)[CH2:6][CH2:7][CH2:8][C:9]([OH:12])([CH3:11])[CH3:10].CC(C)=O>CS(C)=O>[CH3:4][C@@H:5]([C@@H:13]1[C@@:17]2([CH3:33])[CH2:18][CH2:19][CH2:20]/[C:21](=[CH:22]\[CH:23]=[C:24]3\[CH2:25][C@@H:26]([OH:32])[CH2:27][CH2:28][C:29]\3=[CH2:30])/[C@@H:16]2[CH2:15][CH2:14]1)[CH2:6][CH2:7][CH2:8][C:9]([OH:12])([CH3:10])[CH3:11]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Also, when a mass-production was carried out by varying the kinds of an organic solvent, ethanol showed a calcitriol production yield of 48.45 mg/L, and acetone and DMSO showed calcitriol production yields of 74.87 mg/L and 70.85 mg/L, respectively, and calcifediol production yields of 156.37 mg/L and 141.81 mg/L, respectively. Especially, methanol showed a calcitriol production yield of 90.12 mg/L, and a calcifediol production yield of 166.87 mg/L (see Example 9). Accordingly, it can be seen that the inventive composition including methanol, ethanol, acetone, and DMSO showed a high calcitriol or calcifediol productivity.
Aufarbeitung
- customyields of 74.87 mg/L and 70.85 mg/L
Quellen und Nachweise
- ORD-Eintrag
- ord-361d423c474e44afb7ab249f0c11104c
- Quelldatensatz
- uspto-grants-2013_09
- Patentnummer
- US08530205B2
Verknüpfte Notizen
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