Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2399138생성일: 2026년 10월 25일
Ethanol → 2,2'-[Ureylenebis(m-phenylenecarbonylimino)]di-1,5-naphthalenedisulfonic acid tetrasodium salt
https://huagongshe.com/reaction/2399138
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 2-(m-Aminobenzamido)-1,5-naphthalenedisulfonic acid disodium salt | HCID 88828600 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2,2'-[Ureylenebis(m-phenylenecarbonylimino)]di-1,5-naphthalenedisulfonic acid tetrasodium salt | HCID 131710805 | — |
반응 단계
To a stirred solution of 10.0 g of 2-(m-aminobenzamido)-1,5-naphthalenedisulfonic acid disodium salt prepared as in Example 2) and 22.4 g of anhydrous sodium carbonate in 250 ml of water is bubbled in phosgene at room temperature for 35 minutes before a thick translucent gel is formed. The gas diffuser is removed and stirring speed is increased considerably. The resulting mixture is changed to a white solid after about 20 minutes of stirring (at this point the mixture is not acid to Congo Red). The gas diffuser is reinserted and phosgenation is continued for an additional hour at room temperature then the acid mixture is neutralized with 12 ml of 3N sodium hydroxide. The mixture is then filtered over a 48 hour period to obtain a moist paste which is slurried with about 125-150 ml of 80% ethyl alcohol then is filtered and is oven dried at 120° C. overnight to give the product of the example.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04027038 |
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| 출처 데이터셋 | uspto-grants-1977_05 |
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| ORD ID | ord-edb8f56884d94e7a97c1e66be6eb886f |
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| 출처 메모 | uspto-grants-1977_05 |
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