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HRID 41854作成日:2026年10月26日

Carbon Dioxide → 3-Fluoro-4-(pentafluoroethyl)benzoic acid

https://huagongshe.com/reaction/41854

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物WaterHCID 962—
反応物4-Bromo-2-fluoro-1-(pentafluoroethyl)benzeneHCID 86661427—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物3-Fluoro-4-(pentafluoroethyl)benzoic acidHCID 86661428—

反応条件

温度-10 °C

反応手順

A solution of 16.0 g (99% by weight; 54.1 mmol) of 3-fluoro-4-(pentafluoroethyl)-bromobenzene in 110 ml of THF was cooled to −10° C. Added dropwise over the course of 30 minutes were 36.8 ml of a 2M (73.6 mmol) solution of isopropyl-magnesium chloride. The mixture was stirred at −10° C. for 2.5 hours and then cautiously poured onto an excess of dry ice. For working up, 130 ml of water were added, and the mixture was subsequently extracted once with 10 ml of diethyl ether. The aqueous phase was acidified with half-concentrated hydrochloric acid and then extracted with four times 150 ml of diethyl ether. The combined organic phases were dried and the filtrate was freed from the solvent. The residue was recrystallized from CHCl3, giving 10.7 g of product with a purity of 98% by weight.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536097B2
出典データセットuspto-grants-2013_09
ORD IDord-1bced423ecf8465faa3d42167c5b41cd
出典メモuspto-grants-2013_09