Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
6-Amino-2-naphthalenesulfonic acid → 2-Naphthalenesulfonic acid, 6-(acetylamino)-
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 6-Amino-2-naphthalenesulfonic acid | HCID 7116 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 생성물 | 2-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04908478 |
| 출처 데이터셋 | uspto-grants-1990_03 |
| ORD ID | ord-7c739d547f4e4bfd8f575410df807b8b |
| 출처 메모 | uspto-grants-1990_03 |