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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1165360생성일: 2026년 10월 26일

6-Amino-2-naphthalenesulfonic acid → 2-Naphthalenesulfonic acid, 6-(acetylamino)-

https://huagongshe.com/reaction/1165360

반응식

참여 물질

역할이름HCID투입량
반응물6-Amino-2-naphthalenesulfonic acidHCID 7116—
반응물Acetic AnhydrideHCID 7918—
반응물Sodium HydroxideHCID 14798—
생성물2-Naphthalenesulfonic acid, 6-(acetylamino)-HCID 109713—

반응 단계

The suspension thus obtained [1.20 moles of 2-amino- naphthalene-6(8)-sulfonic acid, pH 0.8] is brought at 70° C. with 245 parts of 33% strength sodium hydroxide solution to pH 7.0 and has added to it 155 parts of acetic anhydride (1.5 moles) in the course of 15 minutes, during which the pH decreases to 3.0 and the Bronner acid goes into solution. The acetylation is quantitative. Salting out gives 289 parts of 2-acetaminonaphthalene-6-sulfonic acid calculated at 100% (1.09 moles which corresponds to 73% of theory based on 2hydroxynaphthalene) having a purity of about 70% (diazotization value after hydrolysis, molecular weight 265.3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04908478
출처 데이터셋uspto-grants-1990_03
ORD IDord-7c739d547f4e4bfd8f575410df807b8b
출처 메모uspto-grants-1990_03