戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1107735作成日:2026年10月26日

18-Crown-6 → 1-(2-Butenyl)-7-(4-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine

https://huagongshe.com/reaction/1107735

反応式

関与物質

役割名称HCID仕込み量
反応物18-Crown-6HCID 28557—
反応物4-Fluorobenzylic alcoholHCID 68022—
反応物Potassium tert-butoxideHCID 23665647—
反応物1-(2-Butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazineHCID 53719624—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2-Butenyl)-7-(4-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazineHCID 5399695463.1%

反応手順

0.85 g (0.0076 mole) of potassium tert-butoxide was added to a solution of 0.48 g-(0.0038 mole) of 4-fluorobenzyl alcohol and 0.08 g (0.0003 mole) of 18-crown-6 in 30 ml of tetrahydrofuran and the mixture was stirred at room temperature for 10 minutes. 0.45 g (0.0019 mole) of 1-(2-butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazine was then added to the mixture and stirred at room temperature for 8 hours. After completion of the reaction, the reaction mixture was poured into ice-water and the aqueous mixture was extracted with dichloromethane. The extract was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography through silica gel using a 4:1 mixture of toluene and ethyl acetate as an eluent. An oily material thus obtained was crystallized in hexane to give 0.39 g of 1-(2-butenyl)-7-(4-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine (cis/trans=13/87) as a pale brown powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06063782
出典データセットuspto-grants-2000_05
ORD IDord-95641fdf7231455cac3415e881af0be1
出典メモuspto-grants-2000_05