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HRID 898890作成日:2026年10月27日

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

https://huagongshe.com/reaction/898890

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl SalicylateHCID 4133—
反応物Potassium CarbonateHCID 11430—
反応物Tert-butyl (4-{2-[(methylsulfonyl)oxy]ethyl}phenoxy)acetateHCID 86600965—
溶媒AcetonitrileHCID 6342—
生成物Methyl 2-{2-[4-(2-tert-butoxy-2-oxoethoxy)phenyl]ethoxy}benzoateHCID 6925930661.1%

反応条件

温度-10 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07351858B2
出典データセットuspto-grants-2008_04
ORD IDord-4ee66a3ce3b14f7784fa4e7440f4e764
出典メモuspto-grants-2008_04