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Dimethyl Disulfide → 3-Methyl-4-(methylthio)anisole

HRID 1892062
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1892062
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[CH3:10].C([Li])CCC.[CH3:16][S:17]SC>C1COCC1>[CH3:10][C:3]1[CH:4]=[C:5]([O:8][CH3:9])[CH:6]=[CH:7][C:2]=1[S:17][CH3:16]
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Komponenten

5

Edukt 3

HCID 12232Dimethyl DisulfideHCID 1179151-Bromo-4-methoxy-2-methylbenzeneHCID 178418339Butyllithium

Produkt 1

HCID 5978063-Methyl-4-(methylthio)anisoleAusbeute 96,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To the cold (−78° C.) solution of 2-bromo-5-methoxy toluene (8 g, 0.04 mol) in dry THF (80 mL) under inert atmosphere, butyl lithium solution (1.6M solution in hexane; 36.8 mL, 0.058 mol) was added dropwise and the mixture was stirred for 1 h at same temperature. Dimethyl disulphide (7.7 mL, 0.08 mol) was then added dropwise and the reaction mixture was allowed to warm to room temperature over a period of 2 h. The reaction mixture was quenched with sat. ammonium chloride solution and extracted in diethyl ether. The combined organic extracts were washed with water and brine and dried. The solvent was evaporated in vacuo to yield 6.5 g of 2-methyl-4-methoxy thioanisole, which was used as such in Step 2 MS m/z 168 (M+).

Aufarbeitung

  1. customThe reaction mixture was quenched with sat. ammonium chloride solution
  2. extractionextracted in diethyl ether
  3. washThe combined organic extracts were washed with water and brine
  4. customdried
  5. customThe solvent was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-fc5ab9c5daf240d9af6187c79c670ea8
Quelldatensatz
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08507509B2

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