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HRID 1921915作成日:2026年10月27日

Dimethyl Sulfate → Methyl 2-methoxy-3-methylbenzoate

https://huagongshe.com/reaction/1921915

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfateHCID 6497—
反応物3-Methylsalicylic AcidHCID 6738—
反応物Potassium CarbonateHCID 11430—
溶媒AcetoneHCID 180—
生成物Methyl 2-methoxy-3-methylbenzoateHCID 13229229—

反応手順

To a mixture of 3-methyl-salicylic acid (200 g, 1.32 mol), anhydrous potassium carbonate (500 gram, 3.6 mol) and dry acetone (3.5 L) in a 5 liter round bottle flask, dimethylsulfate (DMS, 210 mL, 2.2 mol) was added in several portions. After stirring at room temperature overnight, the mixture was heated at reflux, and the reaction was monitored by TLC. In order to complete the etherification, further additions of DMS and K2CO3 may be necessary. When TLC indicated the completion of the reaction, the mixture was refluxed 4 more hours to destroy any remaining DMS. The mixture was filtered, and the filtrate was evaporated to remove the solvents. A pale yellow thick oil was obtained as the raw product, yield 215 g (91%). 1H NMR (500 MHz, CDCl3, 25° C.) δ: 2.26 (s, 3H, CH3), 3.78 (s, 3H, OCH3), 3.85 (s, 3H, OCH3), 6.98 (t, J=7.5, 1H, ArH), 7.27 (d, J=7.5, 1H, ArH), 7.58 (d, J=7.5, 1H, ArH); 13C NMR (500 MHz, CDCl3, 25° C.) δ: 15.7, 51.8, 61.1, 123.2, 124.3, 128.8, 132.4, 134.8, 158.1, 166.6.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08173800B2
出典データセットuspto-grants-2012_05
ORD IDord-28af11f704094426a869ba0dc6830139
出典メモuspto-grants-2012_05