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HRID 227369作成日:2026年10月26日

Triethylamine → (1-Methylpiperidin-2-yl)methyl methanesulfonate

https://huagongshe.com/reaction/227369

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物1-Methyl-2-piperidinemethanolHCID 89394—
溶媒TetrahydrofuranHCID 8028—
生成物(1-Methylpiperidin-2-yl)methyl methanesulfonateHCID 44627021—

反応条件

温度0 °C

反応手順

To a solution of 1-methyl-2-piperidine-methanol (Aldrich, 0.27 mL, 2.1 mmol) in 10 mL tetrahydrofuran (THF) at 0° C. was added triethylamine (0.87 mL, 6.22 mmol) followed by methanesulfonyl chloride (0.24 mL, 3.1 mmol). The mixture was stirred at 0° C. for 10 min then the ice-bath was removed and the reaction mixture was stirred at 23° C. for an additional 1.5 h. The reaction mixture was filtered though Celite with THF and concentrated under reduced pressure. This crude material was used directly in the next reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560481B2
出典データセットuspto-grants-2009_07
ORD IDord-a17f828435f94eff96c61b543cf3d75e
出典メモuspto-grants-2009_07