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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230455생성일: 2026년 10월 25일

Hydrochloric Acid → 2-(2,2,2-Trifluoro-1-hydroxy-ethyl)-6-trifluoromethyl-1H-benzimidazole-5-carbonitrile

https://huagongshe.com/reaction/230455

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물3,3,3-Trifluoro-2-hydroxypropanoic acidHCID 244896—
반응물Sodium BicarbonateHCID 516892—
반응물4,5-Diamino-2-(trifluoromethyl)benzonitrileHCID 52991926—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-(2,2,2-Trifluoro-1-hydroxy-ethyl)-6-trifluoromethyl-1H-benzimidazole-5-carbonitrileHCID 86635047—

반응 조건

온도108 °C

반응 단계

4,5-Diamino-2-trifluoromethyl-benzonitrile (4.14 g; 20.6 mmoles) and 3,3,3-trifluoro-2-hydroxy-propionic acid (4.50 g; 31.2 mmoles) were suspended in 6N HCl (7 mL; 42 mmoles) under a nitrogen atmosphere. The reaction was stirred vigorously and heated to 108° C. for 18 hrs, then cooled to room temperature. The reaction was diluted with water (100 mL) and with ethyl acetate (100 mL), then sodium bicarbonate (5.19 g; 62.0 mmoles) was added slowly and in portions to quench the reaction. The aqueous layer was separated and extracted with ethyl acetate (3×40 mL). The extracts were combined, washed with water (30 mL) and brine (30 mL), then dried over Na2SO4. The filtrate was concentrated in vacuo to yield a crude dark solid which was then purified by column chromatography (SiO2; 30% ethyl acetate/CH2Cl2) to yield the title compound as a dark brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566733B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-c18a7d1784284cc087d5396fc1692a5b
출처 메모uspto-grants-2009_07