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HRID 1087345作成日:2026年10月26日

Diisopropylamine → Methyl 2-methoxy-3-hydroxy-3-[2-(8-phenyloctyl)phenyl]propanoate

https://huagongshe.com/reaction/1087345

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物Methyl methoxyacetateHCID 80507—
反応物2-(8-Phenyloctyl)benzaldehydeHCID 9817613—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-methoxy-3-hydroxy-3-[2-(8-phenyloctyl)phenyl]propanoateHCID 15617503—

反応手順

To tetrahydrofuran (50 ml), cooled to -78° C. under argon, was added diisopropylamine (5.7 ml, 0.041 mole) followed by n-butyllithium (16 ml, 0.041 mole) slowly. After 15 minutes, methyl methoxyacetate (4.25 g, 0.041 mole) in tetrhydrofuran (10 ml) was added dropwise. The resulting solution was stirred for 30 minutes after which a solution of 2-(8-phenyloctyl)benzaldehyde in tetrahydrofuran (10 ml) was added dropwise. After 2 hours the reaction mixture was quenched with a solution of saturated ammonium chloride and then diluted with ice water. The aqueous layer was extracted with ether. The combined ether extract was washed with 10% sodium hydroxide (ice cold), dried over magnesium sulfate, filtered and evaporated to give the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05034537
出典データセットuspto-grants-1991_07
ORD IDord-13be1b05c4c14dac9708216186f5e413
出典メモuspto-grants-1991_07