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Carbon tetrabromide → HCID 23064812, Verbindung

HRID 1431919
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1431919
Br[C:2]([Br:5])(Br)Br.[CH:6]12[O:14][CH:9]([CH:10](CO)[CH2:11]1)[CH:8]=[CH:7]2.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C(Cl)Cl>[CH:9]12[O:14][CH:6]([CH:11]([CH2:2][Br:5])[CH2:10]1)[CH:7]=[CH:8]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 2650927-Oxabicyclo[2.2.1]hept-5-en-2-ylmethanol

Produkt 1

HCID 23064812HCID 23064812, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Tetrabromomethane (1.161 g, 3.50 mmol) was added to a solution of 7-oxanorborn-2-en-5-ylmethanol (0.305 g, 2.50 mmol, from Example 2) in CH2Cl2 (12.5 ml). The solution was cooled to 0° C. and admixed with triphenylphosphine (1.836 g, 7 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 12 h. The solvent was removed under reduced pressure and the remaining solid was taken up in cyclohexane. The crude product was purified by flash chromatography (using a 98:2 mixture of cyclohexane and ethyl acetate). 0.3 g (59% of theory) of the pure product were obtained. The product was stored under cool conditions with the exclusion of light.

Aufarbeitung

  1. temperatureto warm to room temperature
  2. customThe solvent was removed under reduced pressure
  3. customThe crude product was purified by flash chromatography (
  4. additiona 98:2 mixture of cyclohexane and ethyl acetate)
  5. custom0.3 g (59% of theory) of the pure product were obtained

Quellen und Nachweise

ORD-Eintrag
ord-2de18b58dc1d42b5b73d66ff38800e42
Quelldatensatz
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07612008B2

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