돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1649578생성일: 2026년 10월 26일

Acetic Anhydride → 2,2'-[[2-[(3-Iodo-4-methylphenyl)amino]-2-oxoethyl]-imino]bisacetic acid

https://huagongshe.com/reaction/1649578

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Nitrilotriacetic AcidHCID 8758—
반응물3-Iodo-p-toluidineHCID 118889—
용매PyridineHCID 1049—
생성물2,2'-[[2-[(3-Iodo-4-methylphenyl)amino]-2-oxoethyl]-imino]bisacetic acidHCID 1324524856.4%

반응 조건

온도100 °C

반응 단계

A slurry of 4.78 g of nitrilotriacetic acid in 40 ml of dry pyridine (dried over molecular sieves) is heated to 60° C. Acetic anhydride (2.55 g) is added slowly and the solution is heated to 100° C. After heating for 0.5 hour, the solution is cooled to 40° C. and a solution of 5.8 g of 3-iodo-4-methylaniline in 20 ml of dry pyridine is added over 25 minutes. The solution is heated at 100° C. for 1.0 hour. The reaction is cooled and rotary evaporated to a residue which is dissolved in 65 ml of 10% sodium hydroxide. This solution is extracted twice with 50 ml portions of methylene chloride diluted with 100 ml of distilled water, and neutralized with concentrated HCl to pH 3.2. The crude product is refrigerated for about 16 hours, filtered, washed twice with 50 ml portions of distilled water, and dried under vacuum at 40° C. The crude product (8.0 g) is recrystallized after Darco treatment to yield 5.7 g of product, melting point 213.5°-215.0° C. (dec).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04418208
출처 데이터셋uspto-grants-1983_11
ORD IDord-62d6e1441a1249ac9a5107a72e8e43ae
출처 메모uspto-grants-1983_11