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HRID 41644作成日:2026年10月25日

Methyl chloroformate → Methyl 4-bromothiophene-3-carboxylate

https://huagongshe.com/reaction/41644

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl chloroformateHCID 6586—
反応物3,4-DibromothiopheneHCID 18452—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-bromothiophene-3-carboxylateHCID 1348791754.5%

反応条件

温度2.5 °C

反応手順

A solution of isopropylmagnesium chloride (1.0 g, 9.7 mmol, 1.2 eq.) in THF (5 mL) was added to a solution of 3,4-dibromo-thiophene (2 g, 8.3 mmol, 1.0 eq.) in THF (15 mL), and stirred for 3 hours while the temperature was maintained at 0-5° C. in an ice/salt bath. Methyl chloroformate (1.6 g, 16.9 mmol, 2 eq.) was added dropwise with stirring. The resulting solution was stirred for an additional 16 hours at room temperature. The reaction was then quenched with water (1 mL). The resulting mixture was concentrated under vacuum, then diluted with EtOAc (50 mL). The resulting mixture was washed 1N HCl (1×100 mL) and saturated aqueous NaCl (2×100). The organic layer was concentrated to provide a crude residue, which was applied onto a silica gel column and eluted with EtOAc/PE (1:50) to yield 4-bromothiophene-3-carboxylic acid methyl ester (1.0 g) as a light yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530663B2
出典データセットuspto-grants-2013_09
ORD IDord-c217fb16a7c64c86b4269c269401a79b
出典メモuspto-grants-2013_09