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HRID 39124作成日:2026年10月23日

Acetonitrile → 1,3-Benzodioxole-5-carboxylic acid, 2,2-difluoro-, methyl ester

https://huagongshe.com/ja/reaction/39124

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物TriethylamineHCID 8471—
反応物5-Bromo-2,2-difluoro-1,3-benzodioxoleHCID 2736271—
触媒HCID 178418397HCID 178418397—
溶媒MethanolHCID 887—
生成物1,3-Benzodioxole-5-carboxylic acid, 2,2-difluoro-, methyl esterHCID 59129261212.8%

反応条件

温度75 °C

反応手順

A solution of 5-bromo-2,2-difluoro-benzo[1,3]dioxole (11.8 g, 50.0 mmol) and tetrakis(triphenylphosphine)palladium (0) [Pd(PPh3)4, 5.78 g, 5.00 mmol] in methanol (20 mL) containing acetonitrile (30 mL) and triethylamine (10 mL) was stirred under a carbon monoxide atmosphere (55 PSI) at 75° C. (oil bath temperature) for 15 hours. The cooled reaction mixture was filtered and the filtrate was evaporated to dryness. The residue was purified by silica gel column chromatography to give crude 2,2-difluoro-benzo[1,3]dioxole-5-carboxylic acid methyl ester (11.5 g), which was used directly in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524767B2
出典データセットuspto-grants-2013_09
ORD IDord-06a7fa1d103c457eae0cf1d257839b78
出典メモuspto-grants-2013_09