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HRID 357761作成日:2026年10月26日

Ammonia → Methyl 4-methylthiophene-2-carboxylate

https://huagongshe.com/reaction/357761

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物WaterHCID 962—
反応物Methyl 5-bromo-4-methylthiophene-2-carboxylateHCID 2795489—
触媒ZincHCID 23994—
溶媒Acetic AcidHCID 176—
生成物Methyl 4-methylthiophene-2-carboxylateHCID 277759390.6%

反応手順

5-Bromo-4-methyl-2-thiophenecarboxylic acid (3.33 g) was dissolved in dimethylformamide (50 ml), and potassium carbonate (4.0 g) and iodomethane (4.0 ml) were added. The mixture was stirred at room temperature for 2 hours, diluted with ethyl acetate, washed with 1N hydrochloric acid, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 5-bromo-4-methyl-2-thiophenecarboxylic acid methyl ester (3.47 g). A mixture of 5-bromo-4-methyl-2-thiophenecarboxylic acid methyl ester (2.36 g), zinc powder (1.65 g), acetic acid (10 ml) and water (10 ml) was stirred under reflux for 3 hours. Zinc powder (1 g) and acetic acid (10 ml) were further added. The mixture was stirred under reflux for 1 day, cooled, poured into concentrated aqueous ammonia and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 4-methyl-2-thiophenecarboxylic acid methyl ester (1.42 g). 4-Methyl-2-thiophenecarboxylic acid methyl ester (1.42 g) was dissolved in a mixture of methanol (10 ml) and tetrahydrofuran (30 ml), and 1N aqueous sodium hydroxide (15 ml) was added. The mixture was stirred at room temperature for 1 hour and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with diethyl ether. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 4-methyl-2-thiophenecarboxylic acid (1.16 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05840917
出典データセットuspto-grants-1998_11
ORD IDord-e39cb44c2c214fe18cea3165f6428ddd
出典メモuspto-grants-1998_11