참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Ethyl orthoformate | HCID 31214 | — |
| 반응물 | 4-Bromo-5-nitrothiophene-2-carbaldehyde | HCID 21886281 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 3-Bromo-5-(diethoxymethyl)-2-nitrothiophene | HCID 86703858 | 81.2% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09440954B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-4d4f5ea7519745e492b3a0bb2f41119c |
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| 출처 메모 | uspto-grants-2016_09 |
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