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HRID 14208作成日:2026年10月25日

Methyl 6-methylnicotinate 1-oxide → Methyl 6-(acetoxymethyl)nicotinate

https://huagongshe.com/reaction/14208

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 6-methylnicotinate 1-oxideHCID 15883477—
溶媒Acetic AnhydrideHCID 7918—
生成物Methyl 6-(acetoxymethyl)nicotinateHCID 10353032121.2%

反応手順

To a solution of methyl 6-methylnicotinate (6.05 g) in methylene chloride (100 mL) was added m-chloroperbenzoic acid (77%, 13.5 g). The reaction mixture was stirred at room temperature for 2 h and then diluted with chloroform (100 mL). The mixture was washed successively with aqueous sodium sulfite, saturated sodium bicarbonate, and brine. The organic later was then dried (sodium sulfate), filtered, and concentrated under reduced pressure to provide 6.21 g of methyl 6-methylnicotinate 1-oxide. A solution of methyl 6-methylnicotinate 1-oxide (4.35 g) in acetic anhydride (50 mL) was heated at 120° C. for 2 h and then concentrated under reduced pressure. Purification by flash column chromatography (silica gel, 1:2 to 3:5 ethyl acetate/hexanes) provided 3.3 g of the title compound: 3H NMR (300 MHz, CDCl3) δ 9.18, 8.31, 7.44, 5.29, 3.96, 2.19.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727997B2
出典データセットuspto-grants-2010_06
ORD IDord-0b398d355f3c42a483894cb1fbd37245
出典メモuspto-grants-2010_06