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HRID 407216作成日:2026年10月26日

Water → 4,6-Dibromo-2-chloro-3-(difluoromethoxy)pyridine

https://huagongshe.com/reaction/407216

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物2-Chloro-2,2-difluoroacetophenoneHCID 238296—
反応物4,6-Dibromo-2-chloropyridin-3-olHCID 53485461—
溶媒AcetonitrileHCID 6342—
生成物4,6-Dibromo-2-chloro-3-(difluoromethoxy)pyridineHCID 8667540277%

反応条件

温度100 °C

反応手順

Potassium carbonate (K2CO3; 5.01 g, 36.3 mmol) and H2O (4 mL) were added to a microwave reaction vessel. 4,6-Dibromo-2-chloropyridin-3-ol (0.359 g, 1.25 mmol) was dissolved in CH3CN (4 mL) and added to the microwave reaction vessel. 2-Chloro-2,2-difluoro-1-phenylethanone (0.953 g, 5.00 mmol) was then added, and the microwave reaction vessel was sealed. The reaction mixture was heated with vigorous stirring with a large stir bar in a Biotage microwave reactor at 100° C. for 4 h. (The reaction mixture is biphasic, and the reaction will not proceed to completion without vigorous stirring.) The reaction mixture was then partitioned between EtOAc and H2O. The organic phase was washed once more with H2O, dried and concentrated. The product was redissolved in CH2Cl2 and filtered through short plug of silica gel utilizing CH2Cl2 as the eluting solvent. The eluent was concentrated to provide the title compound as a light yellow low-melting solid (0.325 g, 0.963 mmol, 77%): 1H NMR (300 MHz, CDCl3) δ 7.73 (s, 1H), 6.63 (t, J=73.1, 1H); EIMS m/z 337.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754229B2
出典データセットuspto-grants-2014_06
ORD IDord-543a3dc074304f22a0fb7924904f3e96
出典メモuspto-grants-2014_06