참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl Salicylate | HCID 4133 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Tert-butyl (4-{2-[(methylsulfonyl)oxy]ethyl}phenoxy)acetate | HCID 86600965 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | Methyl 2-{2-[4-(2-tert-butoxy-2-oxoethoxy)phenyl]ethoxy}benzoate | HCID 69259306 | 61.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07351858B2 |
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| 출처 데이터셋 | uspto-grants-2008_04 |
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| ORD ID | ord-4ee66a3ce3b14f7784fa4e7440f4e764 |
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| 출처 메모 | uspto-grants-2008_04 |
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