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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417709생성일: 2026년 10월 24일

1,1,1-Trifluoro-3-iodopropane → 2-Isopropyl-3,6-dimethoxy-5-(3,3,3-trifluoro-propyl)-2,5-dihydro-pyrazine

https://huagongshe.com/ko/reaction/417709

반응식

참여 물질

역할이름HCID투입량
반응물1,1,1-Trifluoro-3-iodopropaneHCID 156165—
반응물2,5-Dihydro-2-isopropyl-3,6-dimethoxypyrazineHCID 3800909—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-Isopropyl-3,6-dimethoxy-5-(3,3,3-trifluoro-propyl)-2,5-dihydro-pyrazineHCID 6662120259%

반응 조건

온도-78 °C

반응 단계

To a stirred solution of 2-isopropyl-3,6-dimethoxy-2,5-dihydro-pyrazine (1 mL, 5.58 mmol) in THF (13.5 mL) under argon at −78° C. was added a solution of n-butyllithium (2.5 M, 2.3 mL, 5.75 mmol). The solution was stirred at −78° C. for 30 minutes. A solution of 1-Iodo-3,3,3-trifluoropropane (925 μL, 5.87 mmol) in THF (11.5 mL) was added slowly. The resulting solution was stirred at −78° C. for 5 hours, warmed to room temperature and diluted with ethyl acetate. The organic layer was washed successively with saturated aqueous NH4Cl solution, water and brine. The organic layer was then dried (MgSO4), concentrated and purified by flash chromatography to yield 2-Isopropyl-3,6-dimethoxy-5-(3,3,3-trifluoro-propyl)-2,5-dihydro-pyrazine (915 mg, 59%). 1H-NMR: 400 MHz, (CDCl3) δ: 4.04-3.99 (m, 1H), 3.98-3.95 (m, 1H), 3.71 (s, 3H), 3.68 (s, 3H), 2.29-2.20 (m, 1H), 2.18-2.04 (m, 3H), 1.94-1.84 (m, 1H), 1.03 (d, J=6.9 Hz, 3H), 0.71 (d, J=6.8 Hz, 3H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088368B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-595963bbda0140109dbe4f59f42aa937
출처 메모uspto-grants-2012_01