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HRID 582771作成日:2026年10月26日

Hydrochloric Acid → n-(2-Bromo-5-isopropyl-4-nitrophenyl)-4-methylbenzenesulphonamide

https://huagongshe.com/reaction/582771

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物BromineHCID 24408—
反応物Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-HCID 69772—
反応物HCID 178418918HCID 178418918—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒TriethylamineHCID 8471—
生成物n-(2-Bromo-5-isopropyl-4-nitrophenyl)-4-methylbenzenesulphonamideHCID 22111869—

反応条件

温度-30 °C

反応手順

A solution of 23.47 g of N-(4-nitrophenyl)-4-methylbenzenesulphonamide in 230 ml of THF is cooled to -30° C., 100 ml of a 2M solution of isopropylmagnesium chloride in ether is added and the mixture is left stirring for 30 minutes at -30° C. 10.3 ml of bromine are then added at -30° C., the mixture is left stirring for 15 minutes at this temperature and the temperature is then allowed to rise to 20° C. 55 ml of triethylamine are then added and the mixture is left stirring for 1 hour at RT. Water is added, the mixture is acidified to pH 3-4 by adding 10% HCl solution, the organic phase is separated after settling has taken place, the aqueous phase is extracted with ether and the combined organic phases are dried over Na2SO4. The organic phase is stirred in the presence of animal charcoal, filtered and concentrated under vacuum. The residue is taken up in EtOH and the crystallized product formed is drained. 11.6 g of the expected product are obtained, m.p.=132° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05925661
出典データセットuspto-grants-1999_07
ORD IDord-8e81096a567346fb902c19695c444b11
出典メモuspto-grants-1999_07