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HRID 1917513作成日:2026年10月25日

Methanol → Butanoic acid, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-hydroxy-, methyl ester, (S)-

https://huagongshe.com/reaction/1917513

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Potassium CarbonateHCID 11430—
反応物(S)-2-(tert-Butyldimethylsilyloxy)-g-butyrolactoneHCID 10965951—
生成物Butanoic acid, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-hydroxy-, methyl ester, (S)-HCID 11107713—

反応手順

To a solution of (S)-3-(tert-butyldimethylsilyloxy)dihydrofuran-2(3H)-one (91b, 6 g, 27.8 mmol) in methanol (40 mL) was added potassium carbonate (500 mg, 3.6 mmol). The reaction was refluxed overnight. The methanol was removed in vacuo and the residue partitioned between ethyl acetate and water. The organic phase was washed with H2O×2 and dried over anhydrous sodium sulfate. The solvent was removed in vacuo to yield (S)-methyl 2-(tert-butyldimethylsilyloxy)-4-hydroxybutanoate (91c, 3.9 g, 15.7 mmol) as a clear oil. [M+H] calc'd for C11H24O4Si, 249; found, 249.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08618290B2
出典データセットuspto-grants-2013_12
ORD IDord-6d0eae1174934a4b8a7f33756245f8a5
出典メモuspto-grants-2013_12