돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1448504생성일: 2026년 10월 26일

Hydrochloric Acid → 8-(3-Nitro-p-toluamido)-1,3,5-naphthalenetrisulfonic acid

https://huagongshe.com/reaction/1448504

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물8-Aminonaphthalene-1,3,5-trisulfonic acidHCID 87355—
반응물TartrazineHCID 164825—
반응물Sodium AcetateHCID 517045—
반응물4-Methyl-2-nitrobenzoyl chlorideHCID 3016522—
반응물Sodium Acetate TrihydrateHCID 23665404—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물8-(3-Nitro-p-toluamido)-1,3,5-naphthalenetrisulfonic acidHCID 57288108872.9%

반응 단계

To a stirred solution of 22.5 g of 8-amino-1,3,5-naphthalenetrisulfonic acid, trisodium salt in 160 ml of water is added 11.0 g of the preceding product with a small amount of ether. Stirring is continued, and after one hour 1.0 g of sodium acetate trihydrate and 1.0 g of 3-nitro-p-toluoyl chloride are added. The mixture is stirred an additional 3 hours and the above addition of sodium acetate and 3-nitro-p-toluoyl chloride is repeated. The mixture is stirred an additional hour, acidified to Congo Red indicator paper with hydrochloric acid and filtered. The filtrate is neutralized with sodium hydroxide, concentrated, dissolved in 50 ml of water and added to one liter of ethanol with stirring for 16 hours. The solid is filtered and forms a gel on washing with ethanol. The gel is dissolved in water and evaporated. The residue is dissolved in 35 ml of hot water and 320 ml of absolute ethanol is added with stirring. The mixture solidifies and water is added to allow filtration. The solid is washed with ether and dried in vacuo. The filtrate is treated by stirring with one liter of ethanol, the separated solid is collected, washed with ether, and dried to yield a combined total of 23.9 g of 8-(3-nitro-p-toluamido)-1,3,5-naphthalenetrisulfonic acid, trisodium salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04180587
출처 데이터셋uspto-grants-1979_12
ORD IDord-6610eb9395544218981b9114b6b5fefb
출처 메모uspto-grants-1979_12