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HRID 25459作成日:2026年10月24日

Monoperoxyphthalic Acid Magnesium Salt → 4-Fluoro-1-methylsulfinyl-2-nitrobenzene

https://huagongshe.com/ja/reaction/25459

反応式

関与物質

役割名称HCID仕込み量
反応物Monoperoxyphthalic Acid Magnesium SaltHCID 10130449—
反応物4-Fluoro-1-(methylsulfanyl)-2-nitrobenzeneHCID 12700911—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物4-Fluoro-1-methylsulfinyl-2-nitrobenzeneHCID 2256734663%

反応条件

温度20 °C

反応手順

4-Fluoro-1-methylsulfinyl-2-nitrobenzene can be obtained in the following way: 4.7 g of magnesium monoperoxyphthalate are added portionwise to a solution, under argon, of 1.9 g of 4-fluoro-1-methylsulfanyl-2-nitrobenzene in 6 ml of methanol and 30 ml of dichloromethane. The reaction mixture is then stirred at a temperature in the region of 20° C. for 3 hours, and is then filtered through sintered glass and the solid is washed with dichloromethane. The filtrate is washed with an aqueous sodium hydrogencarbonate solution then with water, dried over magnesium sulfate, treated with 3S black, filtered and then concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. The residue thus obtained is purified by chromatography on a column of 125 g of silice (particle size 40-63 μm), eluting with pure dichloromethane. The fractions containing the expected product are pooled and concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. 1.3 g of 4-fluoro-1-methylsulfinyl-2-nitrobenzene are thus obtained in the form of a yellow foam (Rf=0.23, silica gel thin layer chromatography, eluent: dichloromethane/ethyl acetate 90/10)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858638B2
出典データセットuspto-grants-2005_02
ORD IDord-d3701a554f694506a5dba40497c51f19
出典メモuspto-grants-2005_02