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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 333362생성일: 2026년 10월 24일

Triethylamine → 2,2-Dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate

https://huagongshe.com/ko/reaction/333362

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물4-Hydroxy-5,5-dimethyl-2(5H)-furanoneHCID 54720139—
용매DichloromethaneHCID 6344—
생성물2,2-Dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonateHCID 5892634889%

반응 조건

온도-78 °C

반응 단계

To a −78° C. stirred solution of 4-hydroxy-5,5-dimethyl-5H-furan-2-one (250 mg, 1.95 mmol) in 18 mL of anhydrous CH2Cl2, was added triethylamine (0.40 mL, 2.9 mmol) and Tf2O (0.49 mL, 2.9 mmol). The reaction was stirred at −78° C. for 30 minutes, and quenched with saturated NH4Cl solution (10 mL). The mixture was warmed up to room temperature and separated. The aqueous layer was extracted with CH2Cl2 (2×20 mL). All organic layers were combined, dried over Na2SO4 and evaporated to brown oil, which was purified by plugging through a short pad of silica gel column with EtOAc/hexanes (1/3). Evaporation of solvents gave 2,2-dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate as a light brown oil (450 mg, 89%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877923B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-31415ca79c424317887fa00da44f25a0
출처 메모uspto-grants-2014_11