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HRID 1105907생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1105907

반응식

참여 물질

역할이름HCID투입량
반응물BenzenesulfonamideHCID 7370—
반응물Thionyl ChlorideHCID 24386—
반응물Sodium hydrideHCID 24758—
반응물4-[15-(Trifluoromethyl)pentadecylamino]benzoic acidHCID 12831610—
용매DichloromethaneHCID 6344—
용매1,2-DimethoxyethaneHCID 8071—
용매DimethylacetamideHCID 31374—
생성물4-[15-(Trifluoromethyl)pentadecylamino]-N-(phenylsulfonyl)benzamideHCID 20549404—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04310545
출처 데이터셋uspto-grants-1982_01
ORD IDord-abef1a72c9f94be292b1b411da05f27d
출처 메모uspto-grants-1982_01