関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Ethyl orthoformate | HCID 31214 | — |
| 反応物 | 4-Bromo-5-nitrothiophene-2-carbaldehyde | HCID 21886281 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 3-Bromo-5-(diethoxymethyl)-2-nitrothiophene | HCID 86703858 | 81.2% |
反応手順
To a solution of 4-bromo-5-nitrothiophene-2-carbaldehyde (Int. 65) (6.981 g, 29.6 mmol) in EtOH (50 ml), ammonium chloride (0.475 g, 8.87 mmol) and triethyl orthoformate (7.39 ml, 44.4 mmol) were added, and the resulting solution was stirred at 60° C. for 14 hours. Additional triethyl orthoformate (7.39 ml, 44.4 mmol) was added, and the mixture was vigorously refluxed for further 2 days. The solvent was evaporated under vacuum and the crude was partitioned between water and EtOAc. The organic phase was washed with brine, dried over sodium sulfate, filtered and evaporated. The crude was purified by chromatography on silica gel cartridge (petroleum ether/EtOAc=9/1) to afford 3-bromo-5-(diethoxymethyl)-2-nitrothiophene (Int. 66) (7.456 g, 24.04 mmol).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09440954B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-4d4f5ea7519745e492b3a0bb2f41119c |
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| 出典メモ | uspto-grants-2016_09 |
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