Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1649579생성일: 2026년 10월 26일
Acetic Anhydride → 2,2'-[[2-[(4-Bromo-3-methylphenyl)amino]-2-oxoethyl]imino]bisacetic acid
https://huagongshe.com/reaction/1649579
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Nitrilotriacetic Acid | HCID 8758 | — |
| 반응물 | 4-Bromo-3-methylaniline | HCID 23359 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 2,2'-[[2-[(4-Bromo-3-methylphenyl)amino]-2-oxoethyl]imino]bisacetic acid | HCID 13245249 | 54.9% |
반응 단계
A slurry of 9.56 g of nitrilotriacetic acid in 80 ml of dry pyridine (dried over molecular sieves) is heated to 55° C. Acetic anhydride (7.66 g) is added and the solution is heated to 100° C. After heating for 0.5 hour, the solution is cooled to 55° C. and 9.30 g of 4-bromo-3-methylaniline is added with a 5 ml pyridine rinse. The solution is heated at 100° C. for 1.0 hour. The reaction is cooled and rotary evaporated to a pasty solid which is dissolved in 120 ml of aqueous ammonium hydroxide (30 ml concentrated ammonium hydroxide/90 ml distilled water). The clear brown solution is extracted with two 100 ml portions of methylene chloride and neutralized to pH 3 with 35 ml of concentrated HCl. The white solid is filtered, washed with three 25 ml portions of cold distilled water, and dried under vacuum for 2.75 hours at 60° C. The crude product (12.9 g) is recrystallized from 360 ml of 50% ethanol to give 9.85 g of product, melting point 206.5°-209.0° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04418208 |
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| 출처 데이터셋 | uspto-grants-1983_11 |
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| ORD ID | ord-6f74a6f587ca4248aaafdb136373b105 |
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| 출처 메모 | uspto-grants-1983_11 |
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