돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68286생성일: 2026년 10월 24일

Trifluoromethanesulfonic anhydride → Methyl 3-(trifluoromethylsulfonyloxy)-pyridine-2-carboxylate

https://huagongshe.com/ko/reaction/68286

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물Methyl 3-Hydroxy-2-pyridinecarboxylateHCID 819341—
용매DichloromethaneHCID 6344—
생성물Methyl 3-(trifluoromethylsulfonyloxy)-pyridine-2-carboxylateHCID 11066008—

반응 조건

온도0 °C

반응 단계

Triflic anhydride (5.0 g, 18.0 mmol) was added dropwise to a cold (0° C.) solution of methyl 3-hydroxypicolinate (2.5 g, 16.3 mmol) and TEA (2.5 mL, 18.0 mmol) in CH2Cl2 (80 mL). The mixture was stirred at 0° C. for 1 h before it was allowed to warm up to room temperature where it stirred for an additional 1 h. The mixture was then quenched with saturated NaHCO3 solution (40 mL) and the organic layer was separated, washed with brine, dried over MgSO4 and concentrated to give methyl 3-(trifluoromethylsulfonyloxy)picolinate (i.e. Cap-174, step a) (3.38 g, 73%) as a dark brown oil (>95% pure) which was used directly without further purification. 1H NMR (300 MHz, CDCl3) δ ppm 8.72-8.79 (1H, m), 7.71 (1H, d, J=1.5 Hz), 7.58-7.65 (1H, m), 4.04 (3H, s). Rt=1.93 min (Cond.-MD1); LC/MS: Anal. Calcd. for [M+H]+ C8H7F3NO5S: 286.00. found: 286.08.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822444B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ab23e92935cc48598f97864bc8f5dcf6
출처 메모uspto-grants-2014_09