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HRID 1183858作成日:2026年10月26日

Triethylamine → 2-(2,3,5-Triflorobenzylidene)-malonic acid dimethyl ester

https://huagongshe.com/reaction/1183858

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl AcetateHCID 8857—
反応物Methanesulfonyl chlorideHCID 31297—
反応物2,3,5-TrifluorobenzaldehydeHCID 2776950—
反応物DimethylmalonatHCID 6946994—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-(2,3,5-Triflorobenzylidene)-malonic acid dimethyl esterHCID 25166801—

反応手順

To a solution of 2,3,5-triflorobenzaldehyde (1.6 g, 10 mmol) and dimethylmalonate (1.2 ml, 10.5 mmol) in anhydrous dichloromethane (20 ml) under N2 at room temperature in a water bath, was added triethylamine (2.1 ml, 15.4 mmol). Methanesulfonyl chloride (1.0 ml, 12.8 mmol) was added at room temperature. The reaction was stirred for 1 hr. Additional triethylamine (2.1 ml, 15.4 mmol) was added. After the mixture was stirred for 3 hr at room temperature, additional methanesulfonyl chloride (0.5 ml, 6.4 mmol) and triethylamine (1.5 ml, 10 mmol) were added. The mixture was stirred for 1 hr. Water (50 ml) and ethyl acetate (50 ml) were added, separated the layers. Aqueous layer was extracted with ethyl acetate (50 ml). The combined organic layer was washed with brine and dried over anhydrous sodium sulfate. It was concentrated to oil (3.5 g) and identified as 2-(2,3,5-triflorobenzylidene)-malonic acid dimethyl ester. 1 H NMR (CDCl3): δ 7.20 (m, 1 H), 6.85 (m, 1 H), 3.88 (s, 3 H), 3.84 (s, 3 H). Mass: [M+1] 243.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08664411B2
出典データセットuspto-grants-2014_03
ORD IDord-abc49e747c804966bc673a6bdc5b5afe
出典メモuspto-grants-2014_03