戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 42142作成日:2026年10月24日

Ammonium Chloride → 5-Bromo-2-(4-methanesulfonylbenzyloxy)pyridine

https://huagongshe.com/ja/reaction/42142

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物2,5-DibromopyridineHCID 69353—
反応物(4-Methanesulfonylphenyl)methanolHCID 3801026—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物5-Bromo-2-(4-methanesulfonylbenzyloxy)pyridineHCID 6708325631%

反応条件

温度0 °C

反応手順

A solution of 2,5-dibromopyridine (474 mg, 2.00 mmol) and 4-(methanesulfonyl)benzyl alcohol (372 mg, 2.00 mmol) in tetrahydrofuran (5 mL) was cooled to −15° C. under N2 and potassium tert-butoxide (1.0M in tetrahydrofuran, 2.2 mL, 2.20 mmol) was added dropwise over 10 minutes. The mixture was stirred at 0° C. for 5.5 hours, poured into saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1) to give the title compound (210 mg, yield 31%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536176B2
出典データセットuspto-grants-2013_09
ORD IDord-c78bc94182cb42c48b59f4800f97a3c8
出典メモuspto-grants-2013_09