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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2297079Erstellt: 25. Oktober 2026

2,5-Dimethylphenol → 4-Chloro-2,5-xylenol

https://huagongshe.com/reaction/2297079

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,5-DimethylphenolHCID 7267—
EduktSulfuryl chlorideHCID 24648—
EduktSodium BisulfiteHCID 23665763—
KatalysatorDiphenyl sulfideHCID 8766—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Chloro-2,5-xylenolHCID 7075697,8%

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

To a solution of 100 g (0.82 mol) of 2,5-xylenol and 0.9 g of diphenyl sulfide in 700 mL of dichloromethane was added a solution of 106 g (0.79 mol) of sulfuryl chloride in 100 mL of dichloromethane, maintaining the temperature at 5-15° C. The mixture was stirred for an additional hour and then poured onto 400 g of ice-water containing 5 g of sodium bisulfite. The layers were separated, and the organic phase was washed with water, dried (MgSO4), and concentrated to dryness. The crude solids were slurried with a minimum amount of hexanes, filtered, and suction-dried to give 121 g (94%) of product, homogeneous by Thin Layer Chromatography (TLC), GC, and 1H-NMR analysis. 1H-NMR (CDCl3) δ 2.18 (s, 3H), 2.27 (s, 3H), 4.61 (s, 1H), 6.63 (s, 1H), 7.07 (s, 1H). Lit (Blackstock, Aust. J. Chem. 1973, 26, 775): mp 74-75° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06489517B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-1aa87337794c4356abec21a45ce0ad11
Quellennotizuspto-grants-2002_12