참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Dichloromaleic anhydride | HCID 70728 | — |
| 반응물 | Methylamine hydrochloride | HCID 6364545 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2,3-Dichloro-N-methylmaleimide | HCID 14293 | — |
반응 단계
A 3L-three-necked flask fitted with a magnetic stir bar, digital thermocouple/thermometer, nitrogen purge and solid addition funnel was charged with 450 g (269.5 mol) of dichloromaleic anhydride, 191 g (282.8 mol) of methylamine hydrochloride and 1.6 L of acetic acid. The reaction mixture was then cooled to 10° C., and 160 g NaOMe added from the solid addition funnel over 1 hour while keeping the temperature between 10-12° C. The reaction mixture was allowed to stir at room temperature for 42 hours (24 hours is sufficient) then heated to 100° C. for 3 hours. HPLC analysis at this time indicated that all the starting material had disappeared. The reaction was cooled to room temperature and 2 L water was added. The mixture was then cooled to 3-10° C. for 1 hour and filtered at 4° C. The solids were then rinsed with 2 L of cold deionized water. The pale yellow solid dried in an air oven overnight to afford 360 g (75%) yield of the titled compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05919946 |
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| 출처 데이터셋 | uspto-grants-1999_07 |
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| ORD ID | ord-649fa3f6f2fe4238a9450b19fa5e0632 |
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| 출처 메모 | uspto-grants-1999_07 |
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