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HRID 68771作成日:2026年10月25日

Sodium Carbonate → 3-Fluoro-4-oxazol-5-yl-benzoic acid

https://huagongshe.com/reaction/68771

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物4-Bromo-3-fluorobenzoic acidHCID 2773341—
反応物5-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(tris(propan-2-yl)silyl)-1,3-oxazoleHCID 44224311—
触媒Palladium ChlorideHCID 24290—
溶媒DimethylformamideHCID 6228—
生成物3-Fluoro-4-oxazol-5-yl-benzoic acidHCID 68290144—

反応条件

温度80 °C

反応手順

A mixture of 4-bromo-3-fluoro-benzoic acid (1.00 g), 5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-2-triisopropylsilanyl-oxazole (1.90 g), PdCl2 [1,1′-bis(diphenylphosphino)-ferrocene]*CH2Cl2 complex (400 mg), and aqueous Na2CO3 solution (2 M; 5.70 mL) in N,N-dimethylformamide (6 mL) is stirred overnight at 80° C. under an argon atmosphere. After cooling to room temperature the reaction mixture is concentrated in vacuo and water is added. The resulting mixture is acidified with hydrochloric acid (4 M; 6 mL) and extracted with ethyl acetate. The combined extracts are washed with brine, dried over MgSO4 and concentrated in vacuo. The residue is triturated with diethyl ether, filtered off and dried to give the title product. LC (method 1): tR=0.87 min; Mass spectrum (ESI+): m/z=208 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822471B2
出典データセットuspto-grants-2014_09
ORD IDord-d82ac1979eda48fe8aed6529bddb05a5
出典メモuspto-grants-2014_09