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Phenethyl bromide → 4-(2-Bromoethyl)benzenesulfonyl chloride

HRID 2360593
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2360593
[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[Cl:10][S:11](O)(=[O:13])=[O:12]>C(Cl)(Cl)Cl>[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([S:11]([Cl:10])(=[O:13])=[O:12])=[CH:6][CH:5]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 7666Phenethyl bromideHCID 24638Chlorosulfonic acid

Produkt 1

HCID 128467754-(2-Bromoethyl)benzenesulfonyl chlorideAusbeute 80,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6212ChloroformLösungsmittel2×

Versuchsvorschrift

To a solution of 2-bromoethylbenzene (10.0 g; 54 mmol) in 16 ml of chloroform placed at a temperature of 0° C. was added dropwise a solution of chlorosulfonic acid (162 mmol, 18.87 g; 10.82 ml) in 11 ml of chloroform. After 15 minutes at 0° C., the reaction was maintained at room temperature for 3 hours. The reaction mixture was poured onto ice, and the aqueous phase was extracted with chloroform. The combined organic phases were washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was evaporated off to give 12.34 g of crude product, which was purified by chromatography on a column of silica, eluting with chloroform (76% yield). The product obtained was used for the following reaction without further purification.

Aufarbeitung

  1. customplaced at a temperature of 0° C.
  2. additionThe reaction mixture was poured onto ice
  3. extractionthe aqueous phase was extracted with chloroform
  4. washThe combined organic phases were washed with saturated sodium chloride solution
  5. dry with materialdried over anhydrous sodium sulfate
  6. customThe solvent was evaporated off

Quellen und Nachweise

ORD-Eintrag
ord-32f1c94e187f430c8540b35bf68c0823
Quelldatensatz
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08686147B2

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