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HRID 231719作成日:2026年10月27日

Pyridine → 1-Methanesulfonyloxy-2,2,5,5-tetramethylcyclopentane

https://huagongshe.com/reaction/231719

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Methanesulfonyl chlorideHCID 31297—
反応物Sodium BicarbonateHCID 516892—
反応物2,2,5,5-Tetramethylcyclopentan-1-olHCID 551696—
溶媒DichloromethaneHCID 6344—
生成物1-Methanesulfonyloxy-2,2,5,5-tetramethylcyclopentaneHCID 1378237528.6%

反応手順

2.84 g of 2,2,5,5-tetramethylcyclopentanol and 3.2 ml of pyridine were dissolved in 20 ml of methylene chloride, and 4.5 g of methanesulfonyl chloride was added thereto. The mixture was stirred at room temperature for 12 hours, and then 50 ml of aqueous saturated sodium hydrogen carbonate solution was added thereto. The mixture was extracted with 50 ml of ethyl acetate, and the organic layer was washed with aqueous 10% copper sulfate solution, and concentrated under reduced pressure. The resulting residue was recrystallized from n-hexane, whereby 1.26 g of 1-methanesulfonyloxy-2,2,5,5-tetramethylcyclopentane was obtained (m.p. 46° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04847390
出典データセットuspto-grants-1989_07
ORD IDord-6c09d014ffb9417a824fddb49fd9c689
出典メモuspto-grants-1989_07