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HRID 449724作成日:2026年10月25日

Chlorotrimethylsilane → 6-Chloro-3-methoxy-4-trimethylsilanyl-pyridazine

https://huagongshe.com/reaction/449724

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物DiisopropylamineHCID 7912—
反応物3-Chloro-6-methoxypyridazineHCID 74403—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒CyclohexaneHCID 8078—
生成物6-Chloro-3-methoxy-4-trimethylsilanyl-pyridazineHCID 10465917—

反応条件

温度-78 °C

反応手順

In a 2-necked round bottom flask under argon placed 4.0476 g of distilled diisopropylamine and 60 mL of tetrahydrofuran (Aldrich, anhydrous, no stabilizer). The mixture was cooled to −78° C., then ca 20 mL of 2.0 M butyl lithium in cyclohexane was added. The mixture was set in an ice bath for 20 minutes, then cooled to −78° C. and a solution of 2.8912 g of 3-chloro-6-methoxy-pyridazine and 3.05 mL of chlorotrimethyl silane in 12 mL of tetrahydrofuran was added over 15 minutes. The mixture was stirred for 2 hours (a deep red color formed, then faded to yellow), then quenched by the addition of 10 mL of saturated sodium dihydrogen phosphate solution. The mixture was taken up in 350 mL of ethyl acetate, washed 1×75 mL brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481540B2
出典データセットuspto-grants-2013_07
ORD IDord-31681f46521a48c08dceb685476077fa
出典メモuspto-grants-2013_07