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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2052453생성일: 2026년 10월 25일

1,3,6-Naphthalenetrisulfonic acid, 8-amino-, sodium salt (1:?) → 8-(4-Nitro-2-sulfobenzamido)-1,3,6-naphthalenetrisulfonic acid tetrasodium salt

https://huagongshe.com/reaction/2052453

반응식

참여 물질

역할이름HCID투입량
반응물1,3,6-Naphthalenetrisulfonic acid, 8-amino-, sodium salt (1:?)HCID 101899—
반응물Sodium Acetate TrihydrateHCID 23665404—
반응물4-Nitro-2-sulfobenzoic anhydrideHCID 57002923—
용매WaterHCID 962—
생성물8-(4-Nitro-2-sulfobenzamido)-1,3,6-naphthalenetrisulfonic acid tetrasodium saltHCID 131711368296.2%

반응 단계

To an ice bath cooled solution (5° C.) of 16.0 g of 8-amino-1,3,6-naphthalenetrisulfonic acid trisodium salt and 6.7 g of sodium acetate trihydrate in 100 ml of water is added 8.8 g of 4-nitro-2-sulfobenzoic acid anhydride. The mixture is stirred vigorously for 10 minutes and is filtered. The filtrate is cooled in an ice bath and diluted with 500 ml of cold ethanol. The mixture is filtered and the product is washed with ethanol and ether and then is dried. The product is dissolved in 50 ml of warm water and is stirred for 10 minutes after the addition of one ml of acetone. The mixture is treated with activated charcoal, filtered through diatomaceous earth and is washed with 20 ml of water. The filtrate is cooled in an ice bath and acidified with 1.5 ml of concentrated hydrochloric acid. The solution is diluted with 500 ml of cold ethanol and the precipitated material is filtered, washed with ethanol followed by ether and dried. The above purification process is repeated without acidification. The product obtained is dried overnight at 110° C. to give 18.5 g of 8-(4-nitro-2-sulfobenzamido)-1,3,6-naphthalenetrisulfonic acid tetrasodium salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04185032
출처 데이터셋uspto-grants-1980_01
ORD IDord-52af5f890a374cc6ba0e14acca3948bf
출처 메모uspto-grants-1980_01