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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230451생성일: 2026년 10월 24일

4-Methoxy-2,2,6,6-tetramethylpiperidinyl-1-oxy → 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone

https://huagongshe.com/ko/reaction/230451

반응식

참여 물질

역할이름HCID투입량
반응물4-Methoxy-2,2,6,6-tetramethylpiperidinyl-1-oxyHCID 125323—
반응물Potassium BromideHCID 253877—
반응물1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanolHCID 11637778—
반응물Sodium HypochloriteHCID 23665760—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanoneHCID 11594370—

반응 단계

1-(5,6-Dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanol (0.29 g; 1.00 mmole), 4-methoxy-2,2,6,6-tetramethyl-1-piperdinyloxy free radical (4-methoxy-TEMPO free radical; 4.4 mg; 0.03 mmoles) and potassium bromide (KBr; 13 mg; 0.11 mmoles) were dissolved in THF (2.9 mL). The reaction mixture was stirred while cooled to −10° C., after 10 min. a sodium hypochlorite solution (bleach; 10-13% aqueous; 2.10 mL; 3.53 mmoles) was added and allowed to stir for 15 min., then warmed to room temperature and stirred for 15 min. The reaction mixture was diluted with water (20 mL) and ethyl acetate (30 mL), the layers were separated and the aqueous layer was extracted with ethyl acetate (3×30 mL). The extracts were combined and washed with water (30 mL) and brine (40 mL), then dried over Na2SO4. The filtrate was concentrated in vacuo and purified by column chromatography (SiO2; 100% ether) to yield the title compound as a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566733B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-5ad2aee07fae4b059fa528ab3e820a87
출처 메모uspto-grants-2009_07