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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2181686생성일: 2026년 10월 27일

Propyne → Methyl 3-prop-1-ynyl-1-benzofuran-5-carboxylate

https://huagongshe.com/reaction/2181686

반응식

참여 물질

역할이름HCID투입량
반응물PropyneHCID 6335—
반응물Tris(1,1-dimethylethyl)phosphineHCID 83681—
반응물Methyl 3-bromo-1-benzofuran-5-carboxylateHCID 22481688—
촉매Bis(benzonitrile)palladium chlorideHCID 498840—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물Methyl 3-prop-1-ynyl-1-benzofuran-5-carboxylateHCID 22481806226%

반응 단계

Methyl 3-bromobenzofuran-5-carboxylate (750 mg, 2.94 mmol) is combined with bis(benzonitrile)palladium dichloride (169 mg, 0.44 mmol), cuprous iodide (19 mg, 0.10 mmol), tri-t-butylphosphine ((10% in hexane) 1.92 ml, 0.95 mmol), and propyne (2 ml, 35 mmol) in 7 ml dry dioxane in 15 ml screw cap pressure tube under nitrogen. The mixture is treated with DIA (494 μL, 3.6 mmol), is stirred overnight at RT, and is diluted with 50 ml EtOAc. The reaction is washed with 4×25 ml 1:1:0.1 H2O/brine/conc. NH4OH, the organic layer is dried (MgSO4), and the volatiles are removed in vacuo. The crude material is chromatographed over 50 g silica gel (230-400 mesh) eluting with 12% EtOAc/hexane. The appropriate fractions are combined and concentrated to give 460 mg (73%) of methyl 3-prop-1-ynyl-1-benzofuran-5-carboxylate as a pale solid. MS for C13H10O3 (EI) m/z (rel. intensity): 214 (M)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06894042B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-ee0a4f95dac3458ca4743e8deb71f3d8
출처 메모uspto-grants-2005_05