戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 571750作成日:2026年10月27日

Potassium Carbonate → 2-Chloro-3-fluoro-5-(2,2,3,3-tetrafluoropropoxy)pyridine

https://huagongshe.com/reaction/571750

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2,2,3,3-Tetrafluoropropyl trifluoromethanesulfonateHCID 3792475—
反応物2-Chloro-3-fluoro-5-hydroxypyridineHCID 40424737—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium BicarbonateHCID 516892—
生成物2-Chloro-3-fluoro-5-(2,2,3,3-tetrafluoropropoxy)pyridineHCID 11773875283%

反応手順

6-Chloro-5-fluoro-pyridin-3-ol (300 mg, 2.03 mmol) is dissolved in DMF (10 mL). Potassium carbonate (562 mg, 4.07 mmol) is added followed by 2,2,3,3-tetrafluoropropyl trifluoromethanesulfonate (591 mg, 2.24 mmol) (For preparation of this reagent, see US2013/143900, Ex 1). The reaction is stirred at room temperature for 18 hours then allowed to stand at room temperature for 4 days. The reaction is diluted with aqueous NaHCO3 and ethyl acetate. The layers are separated and the aqueous layer is extracted with ethyl acetate (2×). The combined organic layers are washed with brine and concentrated. The crude material is purified via silica gel chromatography using a 0-10% ethyl acetate/hexanes gradient to give the title compound (440 mg, 83%). ES/MS (m/e): 262.0 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09029367B2
出典データセットuspto-grants-2015_05
ORD IDord-9c051a0076a041a5b2803ee85616bb22
出典メモuspto-grants-2015_05