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HRID 1869作成日:2026年10月24日

Ammonium Chloride → 2-methyl-3,4,5,6-tetrafluoropyridine N-oxide

https://huagongshe.com/ja/reaction/1869

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物PentafluoropyridineHCID 69690—
反応物2,3,4,5,6-pentafluoropyridine N-oxideHCID 53688737—
反応物HCID 178418373HCID 178418373—
溶媒Diethyl EtherHCID 3283—
生成物2-methyl-3,4,5,6-tetrafluoropyridine N-oxideHCID 70285119—

反応手順

2,3,4,5,6-Pentafluoropyridine (commercially available from Aldich Chemical Co.) is oxidized to the corresponding N-oxide following the procedures described in Step 6 of Example 66. The 2,3,4,5,6-pentafluoropyridine N-oxide is treated at ambient temperature with one equivalent of methylmagnesium iodide in diethyl ether as described by F. Binns and H. Suschitsky in Chemical Communications, 750-751 (1970) and J Chem Soc (C), 1223-1231 (1771). The reaction mixture is treated with aqueous ammonium chloride and extracted with diethyl ether. The ether solution is dried over anhydrous magnesium sulfate, filtered and concentated under reduced pressure and the crude product is chromatographed on silica gel to afford 2-methyl-3,4,5,6-tetrafluoropyridine N-oxide (3,4,5,6-tetrafluoro-2-picoline). The N-oxide is then reduced to afford the title compound by the procedures described in Step 8 of Example 66.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726182
出典データセットuspto-grants-1998_03
ORD IDord-d1624c7c809f4abaa8b97cad497ea554
出典メモuspto-grants-1998_03