참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Oxalic Acid | HCID 971 | — |
| 반응물 | Acrylic Acid | HCID 6581 | — |
| 반응물 | Bisisopropenyl ether | HCID 13483800 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Acrylic anhydride | HCID 74919 | — |
반응 단계
Acrylic acid (1.47 g, 0.02 mole), diisopropenyl ether (0.99 g, 0.01 mole) and oxalic acid (0.008 g, 8.9×10-5 moles) were mixed in a nitrogen-filled 10-ml volumetric flask. A 30-μl aliquot of this mixture was transferred to a nuclear magnetic resonance tube, mixed with CDCl3 (0.5 ml), methylene chloride (10 μ) and tetramethylsilane. After 24.5 hours, the sample in the nuclear magnetic resonance tube showed that the reaction was almost complete as the acid was nearly consumed. The amount of acrylic anhydride produced was 1.5:1 to that of the 2,2-propane diacrylate. Conversely the mixture in the original volumetric flask had a much lower conversion of reactants to products and almost no anhydride. After 14 days, the amount of acrylic anhydride in the nuclear magnetic resonance tube increased while that in the volumetric flask did not. The ratio of acrylic anhydride to 2,2-propane diacrylate was 3.3:1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04654174 |
|---|
| 출처 데이터셋 | uspto-grants-1987_03 |
|---|
| ORD ID | ord-3368044ebe81404793d63d2bc170c085 |
|---|
| 출처 메모 | uspto-grants-1987_03 |
|---|