돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 898890생성일: 2026년 10월 26일

Methyl Salicylate → Methyl 2-{2-[4-(2-tert-butoxy-2-oxoethoxy)phenyl]ethoxy}benzoate

https://huagongshe.com/reaction/898890

반응식

참여 물질

역할이름HCID투입량
반응물Methyl SalicylateHCID 4133—
반응물Potassium CarbonateHCID 11430—
반응물Tert-butyl (4-{2-[(methylsulfonyl)oxy]ethyl}phenoxy)acetateHCID 86600965—
용매AcetonitrileHCID 6342—
생성물Methyl 2-{2-[4-(2-tert-butoxy-2-oxoethoxy)phenyl]ethoxy}benzoateHCID 6925930661.1%

반응 조건

온도-10 °C

반응 단계

Methyl salicylate (2.7 ml, 21.187 mmol) was dissolved in acetonitrile, and potassium carbonate (5.856 g, 42.373 mmol) was added. The mixture was cooled to −10° C. then tert-butyl (4-{2-[(methylsulfonyl)oxy]ethyl}phenoxy)acetate was added. The mixture was boiled under reflux for 16 hours, and then the solvent was evaporated under reduced pressure. The residue was dissolved in EtOAc, washed with water and brine, then the organic layer was dried with MgSO4 and the solvent was removed by evaporation. The crude material was purified by flash chromatography (silica gel 60 0.004-0.063 mm) using EtOAc: Toluene 50:50 as the eluant. The fractions which contained the desired product were pooled, and solvent evaporated. This gave 5.0 g of pure product (yield 61.1%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07351858B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-4ee66a3ce3b14f7784fa4e7440f4e764
출처 메모uspto-grants-2008_04