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HRID 357739作成日:2026年10月24日

Methyl 3-bromothiophene-2-carboxylate → 3-Bromothiophene-2-carboxylic acid

https://huagongshe.com/ja/reaction/357739

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-bromothiophene-2-carboxylateHCID 2740074—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium HydroxideHCID 14798—
生成物3-Bromothiophene-2-carboxylic acidHCID 273968897.3%

反応手順

3-Bromo-2-thiophenecarboxylic acid methyl ester (7.74 g) was dissolved in a mixture of methanol (35 ml) and tetrahydrofuran (35 ml), and 1N aqueous sodium hydroxide (53 ml) was added. The mixture was stirred at room temperature for 2 hours and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 3-bromo-2-thiophenecarboxylic acid (7.05 g) as crystals.

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-2e768a02cf3442ff911f2d68e5377a5c
出典メモuspto-grants-1998_11