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Bromine → 2-Bromo-1-(4-iodophenyl)ethanone

HRID 222894
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 222894
[I:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][CH:3]=1.[Br:11]Br>O1CCOCC1>[Br:11][CH2:9][C:8]([C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][CH:4]=1)=[O:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 24408BromineHCID 728691-(4-Iodophenyl)ethan-1-one

Produkt 1

HCID 2565722-Bromo-1-(4-iodophenyl)ethanone

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

A solution of 1-(4-iodophenyl)ethanone (55.9 mmol) in dioxane (160 mL) was cooled to 10° C. Bromine (1.1 equiv, 61.6 mmol) was added dropwise to the reaction mixture. After 10 min, the cooling bath was removed and the reaction mixture was stirred at room temperature. After 1.5 h, the reaction mixture was concentrated in vacuo, poured into water (100 mL), and extracted with (3×100 mL) ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated in vacuo to a tan solid (18.2 g) which was used directly in the next step.

Aufarbeitung

  1. customthe cooling bath was removed
  2. waitAfter 1.5 h
  3. concentrationthe reaction mixture was concentrated in vacuo
  4. additionpoured into water (100 mL)
  5. extractionextracted with (3×100 mL) ethyl acetate
  6. dry with materialThe combined organic layers were dried over sodium sulfate
  7. concentrationconcentrated in vacuo to a tan solid (18.2 g) which

Quellen und Nachweise

ORD-Eintrag
ord-6e339b0dad4f4e0c81bc4965f90a699d
Quelldatensatz
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08207340B2

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