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HRID 595014作成日:2026年10月24日

Carbon Dioxide → 3-Bromo-2,5,6-trifluorobenzoic acid

https://huagongshe.com/ja/reaction/595014

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Hydrochloric AcidHCID 313—
反応物DiisopropylamineHCID 7912—
反応物1-Bromo-2,4,5-trifluorobenzeneHCID 67597—
反応物Lithium diisopropylamideHCID 2724682—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-Bromo-2,5,6-trifluorobenzoic acidHCID 1427882552.3%

反応手順

Step (i) n-Butyllithium (2.5M in hexane, 10.5 mL, 1.1 eq.) was added dropwise over 15 min to a solution of diisopropylamine (4.0 mL, 1.2 eq.) in THF (25 mL) at 0° C. After stirring for 15 min, the LDA solution was added dropwise over 40 min to a solution of 2,4,5-trifluorobromobenzene (5.0 g, 24 mmol) in THF (50 mL) at −78° C. The solution was stirred for 10 min and then transferred to a slurry of dry ice (50 g) in diethylether (65 mL). The reaction was allowed to warm to rt and treated with 1M HCl. The phases were separated and the organic layer extracted with 0.5M NaOH. The basic extracts were acidified to pH 1 with 6M HCl and extracted with diethylether. The combined organic phases were dried over sodium sulfate and evaporated to yield 3-bromo-2,5,6-trifluorobenzoic acid as a white solid (3.2 g, 52%). Step (ii)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242987B2
出典データセットuspto-grants-2016_01
ORD IDord-f458c925287840249be13624f543e5b1
出典メモuspto-grants-2016_01