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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 923688생성일: 2026년 10월 26일

Diethyl Ether → 5,7-Difluoro-1-(triisopropylsilyl)-1H-indole

https://huagongshe.com/reaction/923688

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Ammonium ChlorideHCID 25517—
반응물Triisopropylsilyl chlorideHCID 139400—
반응물5,7-difluoro-1H-indoleHCID 2778730—
용매TetrahydrofuranHCID 8028—
생성물5,7-Difluoro-1-(triisopropylsilyl)-1H-indoleHCID 9041856574.6%

반응 조건

온도-75 °C

반응 단계

N-butyl lithium (2.7 ml, 2.5 M, 6.9 mmol) was added to 10 mL dry THF at −70° C. 5,7-difluoro-1H-indole (1.0 g, 6.5 mmol) in 5 mL THF was added in portions to the this solution and the mixture was stirred for 30 min at −75° C. Triisopropylchlorosilane (1.5 mL, 1.3 g, 6.9 mmol) was added, stirring was continued for 1 h at −75° C. and then the mixture was allowed to warm to −5° C. over 2 h. After treatment with 5 mL sat. NH4Cl, the mixture was mixed with 30 mL ether and the organic phase was washed with 5 mL sat. NaCl, dried (Na2SO4) and evaporated. The product was purified by flash chromatography (SiO2; hexanes) to provide the title compound as a clear oil (1.5 g; 74%): 1H NMR (400 MHz, CDCl3) δ 7.35 (d, J=3.1 Hz, 1H), 7.07 (dd, J=8.7, 2.3 Hz, 1H), 6.69 (m, 1H), 6.59 (t, J=3.1 Hz, 1H), 1.67 (m, 3H), 1.13 (d, J=7.6 Hz, 18H). 19F NMR (376 MHz, CDCl3) δ −120.64, −120.65, −122.49, −122.49. EIMS m/z 309.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09278985B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-767285cbb0fc452fa4ac4ea3d8b0bae8
출처 메모uspto-grants-2016_03