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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 657647생성일: 2026년 10월 24일

Triethylamine → 1-(3-{[4'-(2-Ethoxycarbonylethen-1-yl)biphenyl-4-yl]oxy}propyl)piperidine

https://huagongshe.com/ko/reaction/657647

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl AcrylateHCID 8821—
반응물Tri-o-tolylphosphineHCID 80271—
반응물1-{3-[(4'-Bromobiphenyl-4-yl)oxy]propyl}piperidineHCID 23150313—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
생성물1-(3-{[4'-(2-Ethoxycarbonylethen-1-yl)biphenyl-4-yl]oxy}propyl)piperidineHCID 68908313—

반응 단계

A degazed solution of 1-{3-[(4′-bromobiphenyl-4-yl)oxy]propyl}piperidine (2.8 g), triethylamine (2.8 mL), tri(o-tolyl)phosphine (365 mg), palladium acetate (170 mg) and ethyl acrylate (2.9 mL) in acetonitrile (5 mL) is stirred at a temperature close to 60° C. for one hour, then at room temperature overnight and finally 6 h at a temperature close to 90° C. The solution is concentrated under reduced pressure, redissolved in dichloromethane, filtered and chromatographied over silica gel to give 1.3 g of 1-(3-{[4′-(2-ethoxycarbonylethen-1-yl)biphenyl-4-yl]oxy}propyl)piperidine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076329B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-a5caf81d8889465cb3341f48ea648ec3
출처 메모uspto-grants-2011_12