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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2101412생성일: 2026년 10월 26일

Carbon Tetrachloride → 2-(Chloromethyl)-5-(1,2-oxazol-3-yl)pyridine

https://huagongshe.com/reaction/2101412

반응식

참여 물질

역할이름HCID투입량
반응물Carbon TetrachlorideHCID 5943—
반응물ChlorosuccinimideHCID 31398—
반응물2-Methyl-5-(1,2-oxazol-3-yl)pyridineHCID 59834812—
촉매Benzoyl PeroxideHCID 7187—
용매Ethyl AcetateHCID 8857—
생성물2-(Chloromethyl)-5-(1,2-oxazol-3-yl)pyridineHCID 5983483034%

반응 단계

To a stirring mixture of 3-(6-methylpyridin-3-yl)isoxazole (76 mg, 0.474 mmol) and 6 mL carbon tetrachloride, was added N-chlorosuccinimide (69.7 mg, 0.52 mmol), followed by 3 mg benzoyl peroxide. The reaction mixture was refluxed. Additional N-chlorosuccinimide (40 mg, 0.30 mmol) was added in two portions after stirring 2 h and 4 h. After refluxing for a total of 13 h the reaction mixture was diluted with EtOAc, then washed sequentially with 1 N aq. NaOH solution, water and brine. The organic phase was dried (Na2SO4), filtered and concentrated under reduced pressure. The crude product was purified by automated silica gel chromatography (eluted with ethyl acetate-hexanes) to isolate 31 mg (34%) of the title compound as a white solid. HPLC/MS: retention time=1.77 min, [M+H]+=195.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07572808B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-aba49369da18458998d184dd12aa8a6b
출처 메모uspto-grants-2009_08