戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 28605作成日:2026年10月26日

Potassium Carbonate → 2-Bromo-4-chloro-1-(2,2,2-trifluoroethoxy)-benzene

https://huagongshe.com/reaction/28605

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-Bromo-4-chlorophenolHCID 69670—
反応物2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
溶媒DimethylformamideHCID 6228—
生成物2-Bromo-4-chloro-1-(2,2,2-trifluoroethoxy)-benzeneHCID 22571484108%

反応条件

温度100 °C

反応手順

A mixture of 2-bromo-4-chloro-phenol (2.0 g, 9.6 mmol), trifluoro-methanesulfonic acid 2,2,2-trifluoro-ethyl ester (3.8 g, 16.4 mmol), potassium carbonate (8.0 g, 59 mmol), and N,N-dimethylformaldehyde (80 ml) was heated to 100° C. for 72 hours. After cooling to room temperature, the mixture was concentrated under reduced pressure. The residue was treated with water (150 ml) and extracted with ethyl acetate (160 ml). The organic extract was dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:4) to give 2-bromo-4-chloro-1-(2,2,2-trifluoro-ethoxy)-benzene (3.0 g, 100% yield). 1H NMR (acetone-d6) δ 4.80 (q, 2H, J=8.4 Hz, CH2), 7.28 (d, 1H, J=8.9 Hz, Ar), 7.45 (dd, 1H, J=8.9 Hz, J=2.5 Hz, Ar), 7.69 (d, 1H, J—2.5 Hz, Ar).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419984B2
出典データセットuspto-grants-2008_09
ORD IDord-5dfa535b15fa45bab30e6b895f399d6a
出典メモuspto-grants-2008_09