戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2268455作成日:2026年10月26日

Dimethylformamide → Ethyl 2-(4-benzyloxyphenyl)-3-(6-bromo-2,3,4,5-tetramethoxyphenyl)-2-ethoxycarbonylpropionate

https://huagongshe.com/reaction/2268455

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物Diethyl 2-(4-(benzyloxy)phenyl)malonateHCID 2823246—
反応物1-Bromo-6-bromomethyl-2,3,4,5-tetramethoxybenzeneHCID 18348620—
溶媒WaterHCID 962—
生成物Ethyl 2-(4-benzyloxyphenyl)-3-(6-bromo-2,3,4,5-tetramethoxyphenyl)-2-ethoxycarbonylpropionateHCID 1834865149.6%

反応手順

A DMF (120 ml) suspension of ethyl 2-(4-benzyloxyphenyl)-2-ethoxycarbonylacetate (12.0 g, 35.1 mmols), 1-bromo-6-bromomethyl-2,3,4,5-tetramethoxybenzene (16.9 g, 45.6 mmols) and potassium carbonate (14.5 g, 105 mmols) was stirred at room temperature for 6 hours, and then 1-bromo-6-bromomethyl-2,3,4,5-tetramethoxybenzene (2.60 g, 7.02 mmols) was added thereto stirring was continued at room temperature for further 6 hours. Water was added to the reaction mixture, which was then extracted with diethyl ether. The organic layer was washed with water and a saturated aqueous sodium chloride solution, and then dried. The solvent was evaporated out in vacuo, and the resulting crude product was purified by recrystallization (from hexane-ethyl acetate) to obtain the entitled compound (11.0 g) as crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06326369B1
出典データセットuspto-grants-2001_12
ORD IDord-84c101868c234a6ea17a0a5ae58899ec
出典メモuspto-grants-2001_12