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HRID 904030생성일: 2026년 10월 25일

Hydrochloric Acid → 8-(p-Nitrobenzamido)-1,3,6-naphthalenetrisulfonic acid trisodium salt

https://huagongshe.com/reaction/904030

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Nitrobenzoyl chlorideHCID 8502—
반응물Sodium HydroxideHCID 14798—
반응물1,3,6-Naphthalenetrisulfonic acid, 8-amino-, sodium salt (1:?)HCID 101899—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물8-(p-Nitrobenzamido)-1,3,6-naphthalenetrisulfonic acid trisodium saltHCID 131711367238.6%

반응 단계

To a solution of 27.0 g of 8-amino-1,3,6-naphthalenetrisulfonic acid trisodium salt in 100 ml of water and 60 ml of N sodium hydroxide is added 22.5 g of p-nitrobenzoyl chloride and 30 ml of diethyl ether. The reaction mixture is shaken in a separatory funnel for about 15 minutes, and another 60 ml portion of base is added. After shaking for 15 minutes the procedure is repeated with two additional 60 ml portions of base. The reaction mixture is acidified with 7.5 ml of concentrated hydrochloric acid and diluted with 250 ml of water, then extracted 9 times with 300 ml portions of ether. The aqueous phase is neutralized with 5 N sodium hydroxide and allowed to stand overnight at room temperature, then is filtered through diatomaceous earth. The filtrate is concentrated to a low volume in vacuo at 55°-60° C. The crystalline solid formed is collected by filtration, washed and slurried with absolute ethyl alcohol to yield 28.6 g of 8-(p-nitrobenzamido)-1,3,6-naphthalenetrisulfonic acid trisodium salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04229584
출처 데이터셋uspto-grants-1980_10
ORD IDord-62ed7ee46d4341eeaaae949ff6c0bb21
출처 메모uspto-grants-1980_10