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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76170생성일: 2026년 10월 23일

1-Ethoxy-4-ethynylbenzene → Tert-butyl 1-(4-((4-ethoxyphenyl)ethynyl)phenyl)ethyl-carbamate

https://huagongshe.com/ko/reaction/76170

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethoxy-4-ethynylbenzeneHCID 2775124—
반응물tert-butyl N-(1-(4-bromophenyl)ethyl)carbamateHCID 11983730—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매AcetonitrileHCID 6342—
생성물Tert-butyl 1-(4-((4-ethoxyphenyl)ethynyl)phenyl)ethyl-carbamateHCID 66610473—

반응 조건

온도65 °C

반응 단계

24.6 g (168 mmol) 1-ethoxy-4-ethynyl-benzene, 52.8 g (176 mmol) [1-(4-Bromo-phenyl)-ethyl]-carbamic acid tert-butyl ester (50.2) and 42.6 mL (307 mmol) TEA are added to 400 mL ACN. The mixture is warmed to 65° C. 8.84 g (7.65 mmol) Pd(PPh3)4 and 2.91 g (15.3 mmol) CuI are added and the reaction mixture is stirred at reflux for 2 h. The mixture is cooled to r.t. and the solvent is removed in vacuo. The crude product is purified by column chromatography (hexane/EtOAC 9:1→3:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835472B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c35eeda1cd3e47fda628a35dcc1b3630
출처 메모uspto-grants-2014_09