Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66327생성일: 2026년 10월 26일
1-Naphthalenesulfonic acid, 4-amino-5-hydroxy- → 5-Hydroxy-4-m-nitrobenzamido-1-naphthalenesulfonic acid sodium salt
https://huagongshe.com/reaction/66327
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-Naphthalenesulfonic acid, 4-amino-5-hydroxy- | HCID 6752 | — |
| 반응물 | Benzoyl chloride, 3-nitro- | HCID 8495 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5-Hydroxy-4-m-nitrobenzamido-1-naphthalenesulfonic acid sodium salt | HCID 88743053 | — |
반응 단계
A 43 g portion of recrystallized 8-amino-1-naphthol-5-sulfonic acid is suspended in 80 ml of water and 180 ml of 1N sodium hydroxide is added, then 66.6 g of m-nitrobenzoyl chloride is added all at once, washing in with a small amount of ether. The mixture is shaken for 5 minutes and another 180 ml of 1N sodium hydroxide is added with shaking for 1/2 hour. The latter addition of sodium hydroxide and shaking is repeated two more times. The resulting solution is filtered and the filtrate is made acid to Congo Red with hydrochloric acid, a precipitate forms which is collected by filtration. The solid is stirred with about 500 ml of ether and is filtered. This operation is repeated. The ethereal layer is then removed by vacuum siphoning and the solid is then dissolved in about 350 ml of hot water which is allowed to cool to give the product as a green solid which is collected by filtration. The product is then washed with saturated saline solution, 50% ethyl alcohol, absolute ethyl alcohol and ether.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04131684 |
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| 출처 데이터셋 | uspto-grants-1978_12 |
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| ORD ID | ord-8ee5ce0d1e794df1b81efe9249acb144 |
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| 출처 메모 | uspto-grants-1978_12 |
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