関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | 2-Methoxythiophene | HCID 85610 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | tetrahydrofuran HMPA | HCID 86583969 | — |
| 生成物 | 5-Methoxythiophene-2-carbaldehyde | HCID 15937389 | 72.4% |
反応手順
To a solution of 2-methoxythiophene (79 mg, 0.69 mmol) in 3.5 mL of 9:1 tetrahydrofuran/hexamethylphosphoramide under argon at −78° C. was added n-butyllithium (0.30 mL, 2.5 M in hexanes) dropwise. After stirring at −78° C. for 20 minutes, dimethylformamide (0.27 mL, 3.5 mmol) was added in a single portion and the reaction mixture allowed to warm to room temperature while stirring, before being poured into 25 mL of 1 N hydrochloric acid. Organics were extracted with ether (2×25 mL), dried over magnesium sulfate, filtered and concentrated. The crude residue was subjected to chromatography on silica gel with gradient elution (10-12% ethyl acetate in hexanes) to give 5-methoxy-2-thiophenecarbaldehyde (71 mg, 72%). Used without further characterization.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09315495B2 |
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| 出典データセット | uspto-grants-2016_04 |
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| ORD ID | ord-d506f42182834934ae824f4c1ef0d30d |
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| 出典メモ | uspto-grants-2016_04 |
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