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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2096689생성일: 2026년 10월 23일

2,2-Difluoro-2-(fluorosulfonyl)acetic acid → Ethyl 6-difluoromethoxymethylpyridine-2-carboxylate

https://huagongshe.com/ko/reaction/2096689

반응식

참여 물질

역할이름HCID투입량
반응물2,2-Difluoro-2-(fluorosulfonyl)acetic acidHCID 2737516—
반응물2-Pyridinecarboxylic acid, 6-(hydroxymethyl)-, ethyl esterHCID 10921141—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매AcetonitrileHCID 6342—
생성물Ethyl 6-difluoromethoxymethylpyridine-2-carboxylateHCID 6671837213%

반응 단계

2,2-Difluoro-2-(fluorosulfonyl)acetic acid (495 mL, 4.79 mmol) was added dropwise to a solution of ethyl 6-hydroxymethylpyridine-2-carboxylate (800 mg, 4.79 mmol) and CuI (91 mg, 0.479 mmol) in MeCN (10 mL) at room temperature at a rate to maintain the internal temperature <30° C. The mixture was stirred for a further 20 min at room temperature, poured onto brine/water and extracted with EtOAc (×3). The combined extracts were dried (MgSO4), filtered, evaporated and purified by column chromatography (4:1 to 2:1, isohexane:EtOAc) to give the title compound (130 mg, 13%) as a colorless oil; NMR δH (400 MHz, CDCl3) 8.01 (1H, d, J 7.5 Hz), 7.89 (1H, t, J 7.5 Hz), 7.66 (1H, d, J 7.5 Hz), 6.41 (1H, t, J 74.0 Hz), 5.14 (2H, s), 4.49 (2H, q, J 7.0 Hz), 1.44 (3H, t, J 7.0H); (M+H)+ 232.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08450328B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-4e52014b2cb645bcad48fca25b35790a
출처 메모uspto-grants-2013_05