関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 2,3,5-Trifluorobenzaldehyde | HCID 2776950 | — |
| 反応物 | Dimethylmalonat | HCID 6946994 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(2,3,5-Triflorobenzylidene)-malonic acid dimethyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08664411B2 |
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| 出典データセット | uspto-grants-2014_03 |
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| ORD ID | ord-abc49e747c804966bc673a6bdc5b5afe |
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| 出典メモ | uspto-grants-2014_03 |
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