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Sulfuric Acid → HCID 67099747, Verbindung

HRID 1868736
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1868736
OS(O)(=O)=O.O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.[F:20][C:21]([F:48])([F:47])[C:22]1[CH:23]=[C:24]([C:28]2([C:34]([CH:36]([C:42]([O:44][CH2:45][CH3:46])=[O:43])[C:37](OCC)=[O:38])=[O:35])[CH2:33][CH2:32][O:31][CH2:30][CH2:29]2)[CH:25]=[CH:26][CH:27]=1>>[F:20][C:21]([F:47])([F:48])[C:22]1[CH:23]=[C:24]2[C:25]([C:37]([OH:38])=[C:36]([C:42]([O:44][CH2:45][CH3:46])=[O:43])[C:34](=[O:35])[C:28]32[CH2:33][CH2:32][O:31][CH2:30][CH2:29]3)=[CH:26][CH:27]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 1118Sulfuric AcidHCID 14812Phosphorus oxide (P4O10)HCID 67099793diethyl 2-(4-(3-(trifluoromethyl)phenyl)-tetrahydro-2H-pyran-4-carbonyl)malonate

Produkt 1

HCID 67099747HCID 67099747, VerbindungAusbeute 35,6 %

Versuchsvorschrift

H2SO4 (25 mL, 296 mmol) was cooled to 0° C. and treated with P2O5 (10 g, 70 mmol). The mixture was brought to room temperature and added to diethyl 2-(4-(3-(trifluoromethyl)phenyl)-tetrahydro-2H-pyran-4-carbonyl)malonate (4.27 g, 10 mmol). The reaction mixture was then stirred for 1.5 hours. Ice (H2O) was added, and the aqueous mixture was extracted with EtOAc (2×). The combined organic layers were washed with water (2×) and brine, dried (MgSO4), and concentrated in vacuo to give the crude compound as a brown oil. The crude oil was purified by silica flash chromatography (0-100% DCM/hexane) to give the desired compound as a white solid (1.32 g). MS (m/e)=371.2 (M+H)+.

Aufarbeitung

  1. customwas brought to room temperature
  2. additionIce (H2O) was added
  3. extractionthe aqueous mixture was extracted with EtOAc (2×)
  4. washThe combined organic layers were washed with water (2×) and brine
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customto give the crude compound as a brown oil
  8. customThe crude oil was purified by silica flash chromatography (0-100% DCM/hexane)

Quellen und Nachweise

ORD-Eintrag
ord-a1bb0e6de2a1459fbab306d8682e7a7c
Quelldatensatz
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07635715B2

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