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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350337생성일: 2026년 10월 25일

Water → 1-(Tert-butoxycarbonyl)-2-[2-(4-ethoxycarbonylphenyl)ethynyl]pyrrolidine

https://huagongshe.com/reaction/350337

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ethyl 4-iodobenzoateHCID 142891—
반응물tert-Butyl 2-ethynylpyrrolidine-1-carboxylateHCID 14730283—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매DiisopropylamineHCID 7912—
생성물1-(Tert-butoxycarbonyl)-2-[2-(4-ethoxycarbonylphenyl)ethynyl]pyrrolidineHCID 2351191881%

반응 단계

A suspension of ethyl 4-iodobenzoate (1.7 mL, 10 mmol), Pd(PPh3)4 (578 mg, 0.5 mmol), and CuI (190 mmol, 1 mmol) in i-Pr2NH (20 mL) was stirred for 0.5 hr under N2. To this mixture was added a solution of 1-(tert-butoxycarbonyl)-2-ethynylpyrrolidine (1.95 g, 10 mmol) in i-Pr2NH (20 mL) for over 10 min. After stirring for 3 hr at room temp, the mixture was poured into H2O and extracted with EtOAc. The extract was washed with brine, dried over MgSO4, and evaporated. The residue was chromatographed on silica-gel with n-hexane-AcOEt (10:1, v/v) as eluent to give 2.77 g (81%) 1-(tert-butyloxycarbonyl)-2-(2-(4-ethoxycarbonylphenyl)ethynyl) pyrrolidine as a colorless oil. 1H-NMR (CDCl3) δ 1.37 (3 H, t, J=6.8 Hz), 1.49 (9 H, s), 1.85–2.12 (4 H, m), 3.37–3.51 (2 H, m), 4.37 (2 H, q, J=6.8 Hz), 4.54–4.77 (1 H, m), 7.44 (2 H, d, J=7.8 Hz), 7.96 (2 H, d, J=7.8 Hz)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179819B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-8c91533897ca4fedaf41f96cd39e04ce
출처 메모uspto-grants-2007_02