참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | Bicyclo[2.2.1]hept-2-ene, 5-butyl- | HCID 168020 | — |
| 반응물 | 5-Norbornene 2-allylacetate | HCID 86597587 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-Norbornene 2-allylacetate 5-butylnorbornene | HCID 86603900 | — |
반응 단계
5-norbornene-2-allylacetate (NB—CH2—O—C(O)—CH3) (5 mL, 30.9 mmol), 5-butylnorbornene (1.3 mL, 7.7 mmol), and toluene (7.3 mL) were charged into a 250 mL Schlenk flask. Pd(OAc)2 (0.17 mg, 0.77 p mol) and [(Cy)3PH][(B(C6F5)4) (1.48 mg, 1.55 p mol) were dissolved in CH2Cl2 (1 mL) and added to the monomer solution. While the reaction mixture was stirred for 18 hours at 90° C., the reaction mixture became viscous. After the reaction was completed, 120 ml of toluene was added to the viscous solution to dilute it. The solution was poured into an excess of ethanol to precipitate a white polymer, which was filtered through a glass funnel, washed with ethanol, and dried in vacuo at 80° C. for 24 hours to yield 5-norbornene-2-allylacetate/5-butylnorbornene copolymer (4.35 g: 69.2% by weight based on the total weight of used monomers). The weight average molecular weight (Mw) of the copolymer was 303,550 and Mw/Mn was 2.16.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07814713B2 |
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| 출처 데이터셋 | uspto-grants-2010_10 |
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| ORD ID | ord-d61723dacc474dc480954dcbdb26e9bd |
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| 출처 메모 | uspto-grants-2010_10 |
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