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Thionyl Chloride → 4-Bromobenzenesulfinic chloride

HRID 1485628
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1485628
[S:1]([Cl:4])(Cl)=[O:2].[Br:5][C:6]1[CH:11]=[CH:10][C:9](S(O)=O)=[CH:8][CH:7]=1>ClCCl>[Br:5][C:6]1[CH:11]=[CH:10][C:9]([S:1]([Cl:4])=[O:2])=[CH:8][CH:7]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 24386Thionyl ChlorideHCID 27994104-bromobenzenesulfinic Acid

Produkt 1

HCID 109775414-Bromobenzenesulfinic chloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Thionyl chloride (0.53 mL) is added to an ice-cooled solution of 4-bromobenzenesulfinic acid (400 mg) in dichloromethane (15 mL) under an argon atmosphere. The reaction mixture is stirred for 2 h at 0° C., warmed to room temperature, and stirred for an additional 30 min. The mixture is concentrated and the residue is co-evaporated twice with toluene to give crude 4-bromobenzenesulfinic chloride, which is dissolved in tetrahydrofuran (3 mL) and cooled to −78° C. n-Butyllithium (1.6 M in hexane; 2.26 mL) is added to 2,2,2-trifluoroacetamide (205 mg) in tetrahydrofuran (3 mL) at −78° C. and the reaction mixture is stirred for 10 min. The mixture is added to the 4-bromobenzenesulfinic chloride solution at −78° C. and the reaction mixture is stirred for 1 h. The cooling bath is removed and the reaction is quenched by addition of water and brine. The aqueous layer is extracted with ethyl acetate and the combined extracts are washed with brine and concentrated in vacuo to give the title compound which is used for the next step without further purification. LC (method 1): tR=0.92 min; Mass spectrum (ESI+): m/z=314 [M−H]−.

Aufarbeitung

  1. temperaturewarmed to room temperature
  2. stirringstirred for an additional 30 min
  3. concentrationThe mixture is concentrated

Quellen und Nachweise

ORD-Eintrag
ord-c4d3544de5a146ff8fdb5b7d88a3b499
Quelldatensatz
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09422312B2

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