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HRID 1625199作成日:2026年10月25日

Cesium carbonate → 4-Tert-butyl-2-(2-chloro-4-fluorophenoxy)benzoic acid

https://huagongshe.com/reaction/1625199

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物2-Chloro-4-fluorophenolHCID 74814—
反応物2-Bromo-4-tert-butylbenzoic acidHCID 236352—
溶媒TolueneHCID 1140—
生成物4-Tert-butyl-2-(2-chloro-4-fluorophenoxy)benzoic acidHCID 5768770872.2%

反応条件

温度120 °C

反応手順

In a pressure-vessel, a stirring mixture of 2-bromo-4-tert-butylbenzoic acid (1.00 g, 3.89 mmol) and 2-chloro-4-fluorophenol (860 mg, 620 μL, 5.87 mmol) in toluene (20 mL) was added Cs2CO3 (2.53 g, 7.78 mmol) followed by copper(I) triflate benzene complex (98 mg, 0.19 mmol). The sealed vessel was heated to 120° C. for 16 h. After cooling to room temperature, the reaction mixture was partitioned between 50 mL EtOAc and 50 mL H2O. The aqueous layer was acidified using 2.0 N HCl(aq) and re-extracted with EtOAc. The combined organic solution was dried over Na2SO4, filtered, and concentrated. The residue was purified via silica gel chromatography using 0-3% MeOH/CH2Cl2 to give the product, 4-tert-butyl-2-(2-chloro-4-fluorophenoxy)benzoic acid as a white solid (907 mg, 2.81 mmol) in 72% yield. LC/MS: m/z 323.2 (M+H) at 1.99 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08779197B2
出典データセットuspto-grants-2014_07
ORD IDord-729cbca1987243dba6b471d9c68653b3
出典メモuspto-grants-2014_07