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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 531209생성일: 2026년 10월 26일

Acetic Acid → HCID 11137188, 화합물

https://huagongshe.com/reaction/531209

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Acetic AnhydrideHCID 7918—
반응물N-methyliminodiacetic acidHCID 20441—
촉매PyridineHCID 1049—
용매PyridineHCID 1049—
생성물HCID 11137188HCID 1113718877.1%

반응 단계

A round-bottom flask equipped with a PTFE-coated magnetic stir bar was charged with N-methyliminodiacetic acid (25.0 g, 170 mmol, 1.0 equiv), acetic anhydride (85 mL, ˜850 mmol, ˜5 equiv.), and pyridine (274.9 μL, 3.4 mmol, 0.02 equiv). The flask was capped with a rubber septum which was pierced with an 18 gauge needle (alternatively a reflux condensor could be used). The reaction was lowered into a preheated 70° C. oil bath and stirred until the mixture became clear and dark orange (about 1.5 h). The acetic acid, pyridine, and remaining acetic anhydride were then removed by vacuum distillation (37° C. to 42° C. at 30 Torr). The resulting brown-black liquid was azeotroped three times with toluene (50 mL) to remove residual acetic acid and then transferred to an Erlenmeyer flask. To this flask was added enough diethyl ether to dissolve the crude N-methyl morpholine dione product (˜400 mL). The resulting mixture was filtered to remove a black-brown precipitate, and the filtrate was concentrated in vacuo. The resulting pale yellow solid was then recrystallized from a minimum amount of hot diethyl ether to yield N-methyl morpholine dione (MIDA anhydride; 16.9 g, 131 mmol, 77%) as an off-white crystalline solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09353131B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-fcec94dad2064d16895ffa4342188dc0
출처 메모uspto-grants-2016_05