反応 #4450

ord-c6e1cc3c94154c00aca4659516630175

反応方程式

O=C(OO)c1cccc(Cl)c1
m-chloroperbenzoic acid
c1ccc(Cc2nc(-c3ccncc3)cs2)cc1
2-benzyl-4-(4-pyridyl)thiazole
O=C(OO)c1cccc(Cl)c1
m-chloroperbenzoic acid
[O-][n+]1ccc(-c2csc(Cc3ccccc3)n2)cc1
4-[2-(phenylmethyl)-4-thiazolyl]pyridine-1-oxide
収率 95.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGAfter an additional six hours of stirring the mixture
  2. 2
    抽出was extracted with saturated sodium bicarbonate (3×100 mL)
  3. 3
    乾燥The organic layer was dried over sodium sulfate
  4. 4
    濃縮concentrated to a total volume of 75 mL

実験手順

To a suspension of m-chloroperbenzoic acid (14.5 g) in dry methylene chloride (150 mL) was added a solution of 2-benzyl-4-(4-pyridyl)thiazole (15.1 g, 0.06 mol) in methylene chloride (125 mL) over thirty minutes. The mixture was allowed to stir overnight at room temperature then an additional portion of m-chloroperbenzoic acid (3.00 g) was added. After an additional six hours of stirring the mixture was extracted with saturated sodium bicarbonate (3×100 mL). The organic layer was dried over sodium sulfate, and concentrated to a total volume of 75 mL. Dilution with ether (200 mL) afforded 4-[2-(phenylmethyl)-4-thiazolyl]pyridine-1-oxide (15.3 g, 95%). Recrystallization from ethanol/ether afforded an analytical sample. mp. 170°-172° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04725606uspto-grants-1988_02