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HRID 1105907作成日:2026年10月27日

Benzenesulfonamide → 4-[15-(Trifluoromethyl)pentadecylamino]-N-(phenylsulfonyl)benzamide

https://huagongshe.com/reaction/1105907

反応式

関与物質

役割名称HCID仕込み量
反応物BenzenesulfonamideHCID 7370—
反応物Thionyl ChlorideHCID 24386—
反応物Sodium hydrideHCID 24758—
反応物4-[15-(Trifluoromethyl)pentadecylamino]benzoic acidHCID 12831610—
溶媒DichloromethaneHCID 6344—
溶媒1,2-DimethoxyethaneHCID 8071—
溶媒DimethylacetamideHCID 31374—
生成物4-[15-(Trifluoromethyl)pentadecylamino]-N-(phenylsulfonyl)benzamideHCID 20549404—

反応手順

A solution of 31.4 g. of benzenesulfonamide in 250 ml. of dry dimethylacetamide is added dropwise, with stirring and cooling, to a suspension of 5.5 g. of sodium hydride in 100 ml. of dry dimethylacetamide during 30 minutes at room temperature. Stirring is continued for 30 minutes. In the meantime, a mixture of 36.2 g. of 4-[15-(trifluoromethyl)pentadecylamino]benzoic acid in 100 ml. of methylene chloride, 300 ml. of dimethoxyethane, and 40 ml. of thionyl chloride is refluxed for 1 hour and 15 minutes. The solution is evaporated and to the resulting oil residue is added, in one portion, the previously prepared mixture of sodium benzenesulfonamide in dimethylacetamide. The mixture is stirred for 30 minutes, without cooling, and then filtered. The filtrate is poured into 2 liters of water and 250 ml. of saturated sodium chloride solution. The product is collected by filtration and then dissolved in methylene chloride, the mixture is filtered through diatomaceous earth, and brine is added to break the emulsion. The layers are separated, the organic phase is dried and evaporated. The residue is crystallized from toluene to yield the product as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04310545
出典データセットuspto-grants-1982_01
ORD IDord-abef1a72c9f94be292b1b411da05f27d
出典メモuspto-grants-1982_01