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HRID 348921作成日:2026年10月24日

Methyl 3-{[[2-(diethylamino)ethyl](methyl)amino]methyl}-5-methylbenzoate → 3-{[[2-(Diethylamino)ethyl](methyl)amino]methyl}-5-methylbenzoic Acid

https://huagongshe.com/ja/reaction/348921

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-{[[2-(diethylamino)ethyl](methyl)amino]methyl}-5-methylbenzoateHCID 21086144—
溶媒MeOH tetrahydrofuranHCID 21899815—
生成物3-{[[2-(Diethylamino)ethyl](methyl)amino]methyl}-5-methylbenzoic AcidHCID 21085665—

反応手順

A mixture of methyl 3-{[[2-(diethylamino)ethyl](methyl)amino]methyl}-5-methylbenzoate (296 mg, 1.01 mmol) and 3:1:1 methanol/tetrahydrofuran/2 N sodium hydroxide (10 mL) is stirred overnight and then partitioned between ethyl acetate and water. The aqueous layer is acidified to pH 3 with 1 N hydrochloric acid and extracted with chloroform. The aqueous layer is concentrated under reduced pressure to give the title compound. 1H NMR (300 MHz, DMSO-d6) δ 7.99 (s, 1H), 7.82 (s, 1H), 7.80 (s, 1H), 4.56 (m, 2H), 4.31 (m, 2H), 3.98 (m, 2H), 3.17 (m, 4H), 2.51 (s, 3H), 2.50 (s, 3H), 1.27 (m, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07176242B2
出典データセットuspto-grants-2007_02
ORD IDord-5861cd3be476467387489f85889cc879
出典メモuspto-grants-2007_02