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HCID 86700852, Verbindung → HCID 86700854, Verbindung

HRID 881750
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 881750
[Br:1][CH:2]1[C:7]2([C:10]3[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=3)[CH2:8][CH2:9][C:4]([CH:17]=[CH:18][O:19][CH3:20])([CH2:5][O:6]2)[CH2:3]1.[Cr](Cl)([O-])(=O)=[O:22].[NH+]1C=CC=CC=1>ClCCl.O1CCCC1>[CH3:20][O:19][C:18](=[O:22])[CH2:17][C:4]12[CH2:9][CH2:8][C:7]([C:10]3[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=3)([CH:2]([Br:1])[CH2:3]1)[O:6][CH2:5]2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 86700852HCID 86700852, VerbindungHCID 178418287HCID 178418287, Verbindung2×

Produkt 1

HCID 86700854HCID 86700854, VerbindungAusbeute 61 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344DichloromethaneLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a stirred solution of the cis and trans mixtures of 6-bromo-1-(4-chloro-phenyl)-4-(2-methoxy-vinyl)-2-oxa-bicyclo[2.2.2]octane (1.7 g, 4.75 mmol) in dichloromethane (12 ml) and tetrahydrofuran (25 ml) at room temperature, was portionally added pyridinium chlorochromate (3.07 g, 14.26 mmol). The reaction mixture was stirred at room temperature for 2 hours. More pyridinium chlorochromate (2.05 g, 9.51 mmol) was added, and the mixture was stirred for another 60 hours at room temperature. The mixture was filtrated and the filtrate was concentrated, and diluted with ethyl acetate (100 ml). The organic phase was washed with water, brine and dried over Na2SO4, and concentrated. The residue was purified by flash chromatography (heptanes/acetone 2/1) to afford [6-bromo-1-(4-chloro-phenyl)-2-oxa-bicyclo[2.2.2]oct-4-yl]-acetic acid methyl ester (1.08 g, 61%) as colorless oil. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.69-1.79 (m, 1H) 1.87-1.98 (m, 1H) 2.01-2.11 (m, 1H) 2.14 (s, 2H) 2.23-2.30 (m, 1H) 2.52-2.63 (m, 1H) 2.75-2.87 (m, 1H) 3.62 (s, 3H) 3.84 (dd, J=10.11, 2.65 Hz, 2H) 4.19-4.29 (m, 1H) 7.23 (d, J=8.80 Hz, 2H) 7.33 (d, J=8.80 Hz, 2H).

Aufarbeitung

  1. customat room temperature
  2. stirringthe mixture was stirred for another 60 hours at room temperature
  3. filtrationThe mixture was filtrated
  4. concentrationthe filtrate was concentrated
  5. additiondiluted with ethyl acetate (100 ml)
  6. washThe organic phase was washed with water, brine
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated
  9. customThe residue was purified by flash chromatography (heptanes/acetone 2/1)

Quellen und Nachweise

ORD-Eintrag
ord-a7e6c3352f0c4c0a82a2f07812a55500
Quelldatensatz
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08993619B2

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