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HRID 2212558作成日:2026年10月26日

Diethyl dimethylmalonate → 3-(4-Benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl ester

https://huagongshe.com/reaction/2212558

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl dimethylmalonateHCID 15382—
反応物1-Bromo-4-phenylmethoxybenzeneHCID 138835—
反応物CID 53628100HCID 178418400—
溶媒TetrahydrofuranHCID 8028—
生成物3-(4-Benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl esterHCID 6959650850.4%

反応条件

温度-78 °C

反応手順

sec-Butyl lithium (5.85 mL, 7.6 mmol) was added to a solution of 1-bromo-4-benzyloxy-benzene (2.0 g, 7.6 mmol) in THF (10 mL) cooled to −78° C. under nitrogen. The reaction was stirred for 1 h and diethyl dimethylmalonate (4.29 g, 22.8 mmol) was added rapidly. This was stirred for an additional 0.5 h and then allowed to warm to room temperature. The reaction was partitioned between ethyl acetate and 1 N HCl. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated to give an oil. The product was purified by flash column chromatography (FCC) on silica gel eluting hexane:ethyl acetate (90: 10, v:v) to give 3-(4-benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl ester (1.25 g, 50%) as an oil. MS found: (M+H)+=327.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07102008B2
出典データセットuspto-grants-2006_09
ORD IDord-5359d81de4724a08af69adbf01961d95
出典メモuspto-grants-2006_09