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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37224생성일: 2026년 10월 24일

Potassium Iodide → Methyl 2-(4-Tert-Butyldimethylsilyloxymethyl-2-Allylphenoxy)-2-Phenylacetate

https://huagongshe.com/ko/reaction/37224

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물18-Crown-6HCID 28557—
반응물Methyl 2-(2-bromophenyl)acetateHCID 8063364—
반응물4-Tert-butyldimethylsilyloxymethyl-2-allylphenolHCID 19934838—
용매DimethylformamideHCID 6228—
생성물Methyl 2-(4-Tert-Butyldimethylsilyloxymethyl-2-Allylphenoxy)-2-PhenylacetateHCID 1993485165.4%

반응 단계

To a suspension of KH (1.3 eq) in DMF (1 mL) was added a solution of the product of Step C (157 mg, 0.566 mmol) in DMF (1 mL), followed by 18-crown-6 (30 mg; 0.2 eq). The reaction mixture was stirred for 5 minutes at room temperature. A solution of methyl 2-bromophenylacetate (168 mg, 0.735 mmol) in DMF (1 mL) was added, followed by a catalytic amount of potassium iodide. The reaction was heated to 80° C. for 0.5 hours then stirred at room temperature for 16 hours. After concentration in vacuo, the residue was partitioned between water and ethyl acetate. The combined organic layers were washed with water, brine, then dried (MgSO4). After filtration and concentration in vacuo, the residue was chromatographed on silica (MPLC, ethyl acetate/hexanes (5/95)) to afford 158 mg (66%) of the title compound (Rf =0.22, 5% ethyl acetate/hexanes).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420133
출처 데이터셋uspto-grants-1995_05
ORD IDord-c0cc3718b5c04f88bf7fffa683d15765
출처 메모uspto-grants-1995_05