Reaktion #1776

ord-b03b7005ae0f4e16a4358a35620a3d77

Reaktionsgleichung

Cc1ncccc1CO
3-hydroxymethyl-2-methylpyridine
Cc1ncccc1CO
3-Hydroxymethyl-2-methylpyridine
O=S(Cl)Cl
SOCl2
Cc1ncccc1CCl
3-chloromethyl-2-methylpyridine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe solvent and excess SOCl2 were evaporated under reduced pressure
  2. 2
    SonstigeThe residue was partitioned between CH2Cl2 and saturated aqueous NaHCO3
  3. 3
    SonstigeThe organic layer was separated
  4. 4
    Waschenthe aqueous layer was washed with additional CH2 Cl2 (2×40 mL)
  5. 5
    SonstigeThe combined organic layers were evaporated under reduced pressure

Vorschrift

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)).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726172uspto-grants-1998_03