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HRID 216657생성일: 2026년 10월 25일

Propyne → 4-(Tert-butyl-diphenyl-silanyloxymethyl)-2-prop-1-ynyl-pyridine

https://huagongshe.com/reaction/216657

반응식

참여 물질

역할이름HCID투입량
반응물PropyneHCID 6335—
반응물DiethylamineHCID 8021—
반응물TriphenylphosphineHCID 11776—
반응물Sodium BicarbonateHCID 516892—
반응물4-(Tert-butyl-diphenyl-silanyloxymethyl)-2-chloro-pyridineHCID 131729751—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Bis(triphenylphosphine)palladium chlorideHCID 84124—
용매DimethylformamideHCID 6228—
생성물4-(Tert-butyl-diphenyl-silanyloxymethyl)-2-prop-1-ynyl-pyridineHCID 131729750104.4%

반응 조건

온도120 °C

반응 단계

A reaction tube is charged under an atmosphere of argon with 4-(tert-butyl-diphenyl-silanyloxymethyl)-2-chloro-pyridine (9.47 g, 24.79 mmol), palladium(II)-bis(triphenylphosphine)-dichloride (1.78 g, 2.49 mmol, 0.1 equiv), copper(I) iodide (477 mg, 2.49 mmol, 0.1 equiv), and triphenylphosphine (3.94 g, 14.9 mmol, 0.6 equiv). The tube is degassed by alternating three times between vacuum and argon. Diethylamine (39 ml) and N,N-dimethylformamide (2.0 ml), and propyne (50% in THF, 10.1 g, 247 mmol, 10 equiv) are added under an argon atmosphere. The tube is sealed, and the reaction mixture is heated under microwave irradiation for 20 minutes at 120° C. After cooling, the reaction mixture is poured into a semi-concentrated aqueous solution of NaHCO3. After three extractions with EtOAc, the combined organic layers are washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. Purification via flash chromatography (gradient from hexane/EtOAc 100:0 to 50:50) affords the title compound (6.0 g, 63%). 1H NMR (400 MHz, d6-DMSO): δ=8.41 (d, J=5.0 Hz, 1H), 7.57-7.55 (m, 4H), 7.43-7.32 (m, 11H), 7.27 (d, J=5.0 Hz, 1H), 4.72 (s, 2H), 1.99 (s, 3H), 0.98 (s, 9H). MS (ES+): 386 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193236B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-bc6e4e11056541b791e25ed4147f8dbd
출처 메모uspto-grants-2012_06