戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2246657作成日:2026年10月27日

Ethyl trimethylsilylacetate → Ethyl 3-(oxazol-5-yl)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)acrylate

https://huagongshe.com/reaction/2246657

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl trimethylsilylacetateHCID 77687—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物HCID 57835736HCID 57835736—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 3-(oxazol-5-yl)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)acrylateHCID 6868491866.7%

反応条件

温度-78 °C

反応手順

To a solution of lithium bis(trimethylsilyl)amide (31.5 mmol, 1 M in THF) was added ethyl trimethylsilylacetate (31.5 mmol) dropwise at −78° C. After 20 minutes at −78° C., a solution of 5.2 (21 mmol) in THF (60 mL) was added dropwise and the reaction was maintained at −78° C. for 1.5 hours. The reaction was quenched saturated NH4Cl (aq) and warmed to room temperature. The mixture was extracted with EtOAc (500 mL), the organic phase was washed with water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated with silica gel under reduced pressure. The residue was chromatographed (silica gel, 1:1 EtOAc/hexane) to afford compound 5.3 (4.83 g, 14 mmol). MS ESI (pos.) m/e 344.2 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07687526B2
出典データセットuspto-grants-2010_03
ORD IDord-e1e70bfc41fc4b7ba55fd1b7479aeaa6
出典メモuspto-grants-2010_03