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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1828215생성일: 2026년 10월 26일

Stilbene → 1,1-Diphenylethylene

https://huagongshe.com/reaction/1828215

반응식

참여 물질

역할이름HCID투입량
반응물StilbeneHCID 11502—
반응물Benzene, 1,3-bis(1-phenylethenyl)-HCID 118622—
반응물1,4-Bis(1-phenylethenyl)benzeneHCID 5242314—
생성물1,1-DiphenylethyleneHCID 10740—

반응 단계

For instance, in accordance with an embodiment of the present inveniton, a living macrocarbocation, e.g., living cationic polyisobutylene, is reacted with a double diphenylethylene, e.g., 1,3-bis(1-phenylethenyl)benzene (sometimes referred to as meta-double diphenylethylene) or 1,4-bis(1-phenylethenyl)benzene (sometimes referred to as para-double diphenylethylene), to produce a 1,1-diphenylethylene end-functionalized carbocationic polymer. The carbocation is then alkylated with a suitable alkylating agent, e.g., with an organometallic compound such as dimethylzinc, whereupon the resulting macromonomer is readily metallated with a suitable organometallic compound such as an alkyllithium compound, thereby providing a living anionic macroinitiator in near quantitative yield. A sterically hindered lithium compound, e.g., a 1,1-diphenylalkyllithium species, is used in certain embodiments to remove impurities that may be present alongside the 1,1-diphenylethylene end-functionalized polymer, thereby preventing premature termination of the living macroanion.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07056985B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-9fbca44ee16f4ba08f982fb4ed559920
출처 메모uspto-grants-2006_06