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HRID 38225作成日:2026年10月26日

Methanesulfonyl chloride → N-(3-ethynylphenyl)methanesulfonamide

https://huagongshe.com/reaction/38225

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonyl chlorideHCID 31297—
反応物Benzenamine, 3-ethynyl-HCID 104682—
溶媒PyridineHCID 1049—
生成物N-(3-ethynylphenyl)methanesulfonamideHCID 57131399—

反応手順

To a solution of 3-ethynyl aniline (1.05 mL, 10.0 mmol) in pyridine (5 mL) was added methanesulfonyl chloride (857 μL, 1.10 eq.) at a temperature of 0° C. The resulting mixture was stirred overnight at room temperature and was then evaporated. The residue was treated with 2 N aq. HCl (25 mL) and subsequently extracted with ethyl acetate (2×30 mL). The combined organic layers were dried over MgSO4 and evaporated to give the desired methanesulfonamide in quantitative yield. It was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524724B2
出典データセットuspto-grants-2013_09
ORD IDord-e04eb91ca7634a4a97f9b40e63bc61d3
出典メモuspto-grants-2013_09