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HRID 658287作成日:2026年10月24日

Dimethyl malonate → dimethyl (S)-alpha-(1,3-diphenyl-2-propen-1-yl)malonate

https://huagongshe.com/ja/reaction/658287

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl malonateHCID 7943—
反応物Ammonium ChlorideHCID 25517—
反応物Potassium AcetateHCID 517044—
反応物3-Acetoxy-1,3-diphenylpropeneHCID 605877—
反応物N,O-bis(trimethylsilyl)acetamideHCID 6913588—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物dimethyl (S)-alpha-(1,3-diphenyl-2-propen-1-yl)malonateHCID 45115416—

反応手順

In 0.5 ml of dichloromethane were suspended 0.9 mg (2.5 μmol) of [PdCl(η3-C3H5)]2 and 1.8 mg (5.5 μmol) of (R,R)-t-Bu-QuinoxP* (1), followed by stirring at room temperature for 10 to 30 minutes. To the resulting solution were added a solution of 126 mg (0.50 mmol) of 1,3-diphenyl-2-propenyl acetate in 1.5 ml of dichloromethane, 171 μl (1.50 mmol) of dimethyl malonate, 367 μl (1.50 mmol) of N,O-bis(trimethylsilyl)acetamide (BSA), and a trace amount of potassium acetate. The reaction system was stirred at room temperature for 1 hour. The reaction mixture was diluted with diethyl ether, and a saturated aqueous solution of ammonium chloride was added to stop the reaction. The resulting mixture was extracted with diethyl ether, and the organic layer was washed with a sodium chloride aqueous solution. The organic layer was dried over anhydrous sodium sulfate. Any volatile matter was evaporated off, and the residue was purified by silica gel column chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08076480B2
出典データセットuspto-grants-2011_12
ORD IDord-0b47e6b8dd0c4e6cba6470c6760811ac
出典メモuspto-grants-2011_12