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HRID 1172258생성일: 2026년 10월 27일

Tert-Butylamine → t-Butyl 5-(6-hydroxymethylpyridin-2-yl)pent-4-ynoate

https://huagongshe.com/reaction/1172258

반응식

참여 물질

역할이름HCID투입량
반응물Tert-ButylamineHCID 6385—
반응물(6-Bromopyridin-2-yl)methanolHCID 3517811—
반응물4-Pentynoic acid, 1,1-dimethylethyl esterHCID 10877341—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
생성물t-Butyl 5-(6-hydroxymethylpyridin-2-yl)pent-4-ynoateHCID 5810520356.9%

반응 조건

온도80 °C

반응 단계

To a 200 mL round-bottom flask, 3.49 g of 2-bromopyridine-6-methanol, 3.0 g of t-butyl 4-pentynoate, 190 mg of BHT, 1.17 g of copper(I) iodide, 877 mg of tetrakis(triphenylphosphine)palladium(0), 2.72 g of t-butylamine and 56 mL of DMF were added, and the mixture was stirred under argon atmosphere at 80° C. for 6 hours. After the DMF was removed under reduced pressure from the reaction mixture, saturated aqueous sodium bicarbonate was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and then the solvent was removed. The residue was purified by chromatography on silica gel (n-hexane-ethyl acetate=2:1) to give 2.76 g of t-butyl 5-(6-hydroxymethylpyridin-2-yl)pent-4-ynoate as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07834002B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-7e5a40fea3f542e6ad4cf74ba32c9a86
출처 메모uspto-grants-2010_11