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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1160023생성일: 2026년 10월 25일

Ethanol → 5-Norbornene 2-allylacetate 5-butylnorbornene

https://huagongshe.com/reaction/1160023

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물TolueneHCID 1140—
반응물Bicyclo[2.2.1]hept-2-ene, 5-butyl-HCID 168020—
반응물5-Norbornene 2-allylacetateHCID 86597587—
촉매palladium(II) acetateHCID 167845—
용매DichloromethaneHCID 6344—
생성물5-Norbornene 2-allylacetate 5-butylnorborneneHCID 86603900—

반응 조건

온도90 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07814713B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-d61723dacc474dc480954dcbdb26e9bd
출처 메모uspto-grants-2010_10