Sodium Bicarbonate → 17-phenyl-trinor-PGF2alpha isopropyl ester

HRID 599529Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 599529
[Si]([O:8][C@@H:9]([CH2:38][CH2:39][C:40]1[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=1)/[CH:10]=[CH:11]/[C@H:12]1[C@H:16]([O:17][Si](C(C)(C)C)(C)C)[CH2:15][C@H:14]([OH:25])[C@@H:13]1[CH2:26]/[CH:27]=[CH:28]\[CH2:29][CH2:30][CH2:31][C:32]([O:34][CH:35]([CH3:37])[CH3:36])=[O:33])(C(C)(C)C)(C)C.C([O-])(O)=O.[Na+]>CC(O)C>[OH:17][C@@H:16]1[CH2:15][C@H:14]([OH:25])[C@H:13]([CH2:26]/[CH:27]=[CH:28]\[CH2:29][CH2:30][CH2:31][C:32]([O:34][CH:35]([CH3:37])[CH3:36])=[O:33])[C@H:12]1/[CH:11]=[CH:10]/[C@@H:9]([OH:8])[CH2:38][CH2:39][C:40]1[CH:41]=[CH:42][CH:43]=[CH:44][CH:45]=1

Komponenten

4

Versuchsvorschrift

A solution of compound (11b) (60 g) prepared in EXAMPLE 20 and aqueous HF (2N, 135 mL) in IPA (240 mL) was stirred. Saturated aqueous NaHCO3 (120 mL) was added and the mixture was extracted with EtOAc (600 mL). The separated aqueous layer was extracted with EtOAc (300 mL) and the combined organic layer was washed with saturated aqueous NaCl (300 mL), dried with Na2SO4, filtered, and the filter cake was washed with EtOAc (200 mL). The filtrate was concentrated to furnish 43.5 g of crude compound (11c) (84.3% HPLC purity, 84% yield) which was directly used without purification in EXAMPLE 22.

Aufarbeitung

  1. extractionthe mixture was extracted with EtOAc (600 mL)
  2. extractionThe separated aqueous layer was extracted with EtOAc (300 mL)
  3. washthe combined organic layer was washed with saturated aqueous NaCl (300 mL)
  4. dry with materialdried with Na2SO4
  5. filtrationfiltered
  6. washthe filter cake was washed with EtOAc (200 mL)
  7. concentrationThe filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-0db77b0572314e3c8a3fddfbfbcff4ea
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07897795B2

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