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HRID 1357753作成日:2026年10月25日

Methyl morpholine oxide → 3-Methyl-4-nitrobenzaldehyde

https://huagongshe.com/reaction/1357753

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl morpholine oxideHCID 82029—
反応物3-Methyl-4-nitrobenzyl alcoholHCID 591360—
触媒HCID 178419074HCID 178419074—
溶媒DichloromethaneHCID 6344—
生成物3-Methyl-4-nitrobenzaldehydeHCID 1119452874%

反応手順

To a solution of 3-methyl-4-nitrobenzyl alcohol (3.0 g, 18 mmol), N-methylmorpholine-N-oxide (3.2 g, 27 mmol), and powdered 4A molecular sieves (8.98 g) in methylene chloride (40 mL) was added in one portion tetrapropylammonium perruthenate (0.315 g, 0.898 mmol), and the reaction stirred at room temperature. The reaction was filtered through silica gel, eluting with methylene chloride, solvent evaporated and the residue purified by flash chromatography to provide 2.2 g of the title compound. Examp~le 219B 5 9-(3-methyl-4-nitrophenyl)-2,3,5.6,7,9-hexahydrothieno[3.2-b]quinolin-8(4H)-one 1,1-dioxide 3-Methyl-4-nitrobenzaldehyde (0.99 g, 6.0 mmol) was processed according to the method of Example 11 5C to provide the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06593335B1
出典データセットuspto-grants-2003_07
ORD IDord-a7c4f60d6f274b29819e481570559597
出典メモuspto-grants-2003_07