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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450074Generated: October 26, 2026

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

https://huagongshe.com/reaction/1450074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantPentafluoropyridineHCID 69690—
Reactant2,3,4,5,6-pentafluoropyridine N-oxideHCID 53688737—
ReactantHCID 178418373HCID 178418373—
SolventDiethyl EtherHCID 3283—
Product2-methyl-3,4,5,6-tetrafluoropyridine N-oxideHCID 70285119—

Reaction Steps

2,3,4,5,6-Pentafluoropyridine (commercially available from Aldrich 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599816
Source datasetuspto-grants-1997_02
ORD IDord-ce40650efd9a40d686e15056a01deb3d
Source noteuspto-grants-1997_02