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HRID 81339생성일: 2026년 10월 23일

Triethylamine → [4-(4-Cyanophenyl)but-3-ynyl]carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/81339

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-IodobenzonitrileHCID 76467—
반응물tert-Butyl 3-butyn-1-ylcarbamateHCID 10725815—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매TetrahydrofuranHCID 8028—
생성물[4-(4-Cyanophenyl)but-3-ynyl]carbamic acid tert-butyl esterHCID 6736470799%

반응 단계

But-3-ynylcarbamic acid tert-butyl ester (3.66 g, 22 mmol) was added dropwise to an ice cooled, stirring, argon purged mixture of 4-iodobenzonitrile (4.5 g, 19.6 mmol), dichlorobis(triphenylphosphine)palladium(II) (0.69 g, 0.98 mmol), copper (1) iodide (0.19 g, 0.98 mmol), triethylamine (11 mL, 78.4 mmol), and THF (24 mL). After stirring for 10 min, the ice bath was removed, and the reaction was allowed to stir for an additional 2 h. The reaction mixture was passed through a pad of silica gel with methylene chloride/ethyl acetate (5:1) as eluant. After evaporating the solvent, the crude product was chromatographed with methylene chloride/ethyl acetate (20:1) as eluant. Evaporation of the solvent, followed by placement under vacuum for 1 h, afforded the pure product 56 (5.2 g, 99%) as an oil. 1H NMR (300 MHz, CDCl3) δ 1.46 (s, 9H), 2.64 (t, 2H), 3.37 (m, 2H), 4.85 (br s, 1H), 7.47 (d, 2H), 7.58 (d, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846688B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-5e656e4dfbef4f54b82be3b57cef2ec3
출처 메모uspto-grants-2014_09