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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1680Erstellt: 23. Oktober 2026

Thionyl Chloride → 3-(Chloromethyl)-2-methylpyridine

https://huagongshe.com/de/reaction/1680

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThionyl ChlorideHCID 24386—
Edukt(2-Methylpyridin-3-yl)methanolHCID 302564—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(Chloromethyl)-2-methylpyridineHCID 12243711—

Reaktionsschritte

To a stirred solution of 3-hydroxymethyl-2-methylpyridine from Step 1 above (1.00 g, 8.13 mmol) in 40 mL of CH2Cl2 at ambient temperature was added SOCl2 (9.0 mL, 123 mmol). The reaction mixture was stirred for 4 hours, and the solvent and excess SOCl2 were evaporated under reduced pressure. The residue was partitioned between CH2Cl2 and saturated aqueous NaHCO3. The organic layer was separated, and the aqueous layer was washed with additional CH2 Cl2 (2×40 mL). The combined organic layers were evaporated under reduced pressure to give 3-chloromethyl-2-methylpyridine as a pale yellow-brown solid (TLC: Rf =0.85 in 5% MeOH in CH2Cl2 ; FAB MS m/z 142 (M+ +H)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726172
Quelldatensatzuspto-grants-1998_03
ORD IDord-b03b7005ae0f4e16a4358a35620a3d77
Quellennotizuspto-grants-1998_03