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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2210621생성일: 2026년 10월 23일

Ethylenediamine → 2-Amino-1,5-naphthalenedisulfonic acid

https://huagongshe.com/ko/reaction/2210621

반응식

참여 물질

역할이름HCID투입량
반응물EthylenediamineHCID 3301—
반응물2-Amino-5-hydroxynaphthalene-1,7-disulphonic acidHCID 81024—
반응물4,5,6-Trifluoro-1,2,3-triazineHCID 13899144—
반응물DifluorotriazineHCID 19878636—
생성물2-Amino-1,5-naphthalenedisulfonic acidHCID 8338100%

반응 단계

31.9 g of 2-amino-5-hydroxy-naphthalene-1,7-disulphonic acid are subjected to a condensation reaction with trifluorotriazine as described in Example 1. 5.0 g of ethylenediamine are added to the solution of the resulting difluorotriazine compound at 0°, a pH of 5.5-6.5 being maintained. The condensation has ended after 2 to 3 hours. A diazo compound obtained by the customary route by diazotisation of 30.3 g of 2-amino-naphthalene-1,5-disulphonic acid is added to the reaction product of the formula ##STR20## which is largely present as a suspension, the pH simultaneously being kept at pH 7.0-7.5 by sprinkling in sodium bicarbonate. When the coupling has ended, the dyestuff of the formula ##STR21## which has precipitated as a sparingly soluble product, is filtered off with suction and stirred in 1 l of water again. 16.9 g of 2,4,6-trifluoro-5-chloro-pyrimidine are added dropwise at 0°-5°, during which a pH of 7.5-8.0 is maintained with dilute sodium hydroxide solution. The dyestuff dissolves during the condensation reaction. When the condensation has ended (thin layer chromatogram), the dyestuff is salted out, filtered off with suction, dried and ground. The red powder dissolves readily in water and dyes cotton a clear scarlet (colour code number 6).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05459246
출처 데이터셋uspto-grants-1995_10
ORD IDord-a2862839424f4443997a4deed569a808
출처 메모uspto-grants-1995_10