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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45061생성일: 2026년 10월 26일

Imidazole → 3-(tert-Butyl-dimethyl-silanyloxymethyl)-5-trifluoromethyl-phenylamine

https://huagongshe.com/reaction/45061

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물Sodium FluorideHCID 5235—
반응물Ethyl AcetateHCID 8857—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물3-Amino-5-(trifluoromethyl)benzoic acidHCID 609556—
반응물Aluminium lithium hydrideHCID 21226445—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물3-(tert-Butyl-dimethyl-silanyloxymethyl)-5-trifluoromethyl-phenylamineHCID 137329775—

반응 조건

온도0 °C

반응 단계

To a solution of 3-Amino-5-trifluoromethyl-benzoic acid (2.0 g, 9.76 mmol) in THF (40 mL) at 0° C. is added LiAlH4 in THF (1 M, 39 mL). The mixture is warmed to reflux and stirred for 62 h. The mixture is then cooled to 0° C. and NaF (2.2 g) is added followed by H2O (3.8 mL). The slurry is stirred for 10 minutes and then allowed to warm to rt and stir an additional 40 min. The mixture is filtered and the solid is rinsed with EtOAc and MeOH. The filtrate is concentrated and the crude residue is mixed with imidazole (2.66 g, 39 mmol) and DCM (30 mL) at 0° C. TBSCl (3.5 g, 23.4 mmol) is added and the mixture is stirred at rt for 5 h. The reaction mixture is then diluted with EtOAc, washed with saturated aqueous NaHCO3, brine, and dried over Na2SO4. Concentration provides the title compound that is carried on to next step without further purification. MS (ESI) m/z 306.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541432B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-1875c82f897145ed8ba3994b007c15ee
출처 메모uspto-grants-2013_09