Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Maleic Anhydride → 2-Hydroxyethyl oxabicyclo[2,2,1]hept-5-ene-2-carboxylate t-butyl 5-norbornene-2-carboxylate 5-norbornene-2,3-dicarboxylic acid maleic anhydride
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Maleic Anhydride | HCID 7923 | — |
| 반응물 | 5-Norbornene-2,3-dicarboxylic acid | HCID 97965 | — |
| 반응물 | Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 1,1-dimethylethyl ester | HCID 15607334 | — |
| 반응물 | 2-Hydroxyethyl oxabicyclo[2,2,1]hept-5-ene-2-carboxylate | HCID 70179192 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Hydroxyethyl oxabicyclo[2,2,1]hept-5-ene-2-carboxylate t-butyl 5-norbornene-2-carboxylate 5-norbornene-2,3-dicarboxylic acid maleic anhydride | HCID 86758319 | 266.1% |
반응 단계
2-hydroxyethyl oxabicyclo[2,2,1]hept-5-ene-2-carboxylate (0.1 mol), t-butyl 5-norbornene-2-carboxylate (0.85 mol), 5-norbornene-2,3-dicarboxylic acid (0.05 mol) and maleic anhydride (1 mol) were dissolved in a tetrahydrofuran solvent (200 g). 2,2-azobisisobutyonitrile (5.84 g) was added, and the solution was mixed. The solution was polymerized at a temperature of 67° C. in a nitrogen atmosphere for 10 hours. After the polymerization reaction was completed, the polymer was precipitated in an ethyl ether solvent, then dried in a vacuum to obtain the pure title polymer (87.627 g). (yield: 30%, purity: 99.9%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06416926B1 |
| 출처 데이터셋 | uspto-grants-2002_07 |
| ORD ID | ord-116f96f2f9944ac6813a6f6f2777554f |
| 출처 메모 | uspto-grants-2002_07 |