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HRID 37224作成日:2026年10月26日

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

https://huagongshe.com/reaction/37224

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物18-Crown-6HCID 28557—
反応物Methyl 2-(2-bromophenyl)acetateHCID 8063364—
反応物4-Tert-butyldimethylsilyloxymethyl-2-allylphenolHCID 19934838—
溶媒DimethylformamideHCID 6228—
生成物Methyl 2-(4-Tert-Butyldimethylsilyloxymethyl-2-Allylphenoxy)-2-PhenylacetateHCID 1993485165.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420133
出典データセットuspto-grants-1995_05
ORD IDord-c0cc3718b5c04f88bf7fffa683d15765
出典メモuspto-grants-1995_05