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HRID 2395925作成日:2026年10月26日

Aniline → Benzenesulfonamide, 4-methyl-N-phenyl-

https://huagongshe.com/reaction/2395925

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物TriethylamineHCID 8471—
反応物Ethyl acetate hexaneHCID 21226206—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物Benzenesulfonamide, 4-methyl-N-phenyl-HCID 2456—

反応手順

Aniline (1.86 g, 0.02 mol) was dissolved in methylene chloride under nitrogen and triethylamine (3.8 mL, 0.02 mol) was added. This solution wascooled in an ice bath and a solution of p-toluenesulfonyl chloride (3.8 g, 0.02 mol) was added dropwise via a syringe. After stirring this solution for 4 h at room temperature, TLC analysis (silica gel, 20% ethyl acetate/hexane) indicated completion of the reaction. The reaction mixturewas poured into ether and the precipitate filtered. The ether layer was washed with water, dried over MgSO4 and concentrated to yield an oilymaterial. This crude product was chromatographed on silica using 35% ethyl acetate and hexane to obtain a solid which was further recrystallized in methylene chloride/hexane; m.p. 104° C.; 1H NMR (CDCl3) δ2.36 (s, 3H), 7.07-7.25 (m, 8H), 7.67-7.69 (d, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05491072
出典データセットuspto-grants-1996_02
ORD IDord-c252f627c2fd4c92ac36b2911bd08852
出典メモuspto-grants-1996_02