関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Methyl 5-formylthiophene-3-carboxylate | HCID 818925 | — |
| 反応物 | HCID 178418809 | HCID 178418809 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | (+/-)-5-(1-Hydroxy-3,3-dimethyl-butyl)-thiophene-3-carboxylic acid methyl ester | HCID 59355935 | 44.1% |
反応手順
A solution of 5-formyl-thiophene-3-carboxylic acid methyl ester (0.504 g, 2.96 mmol) in Et2O (30 mL) at 0° C. is treated with neopentyl magnesium chloride (7.1 mL, 0.5 M in Et2O, 3.6 mmol) and stirred for 15 min. Solution warmed to rt and additional Et2O (10 mL) added. The reaction mixture is stirred overnight at rt. after which it is poured into H2O (30 mL) and extracted with EtOAc (3×50 mL). Combined extracts washed with brine, dried over MgSO4, filtered, and concentrated. The residue is loaded onto silica gel and eluted using hexanes with an ethyl acetate gradient from 0% to 50%. The resulting mixture is then loaded onto C18 and eluted using H2O and a MeCN gradient from 15% to 100% giving (±)-5-(1-hydroxy-3,3-dimethyl-butyl)-thiophene-3-carboxylic acid methyl ester (0.316 g, 44%) as a light yellow syrup.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08084489B2 |
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| 出典データセット | uspto-grants-2011_12 |
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| ORD ID | ord-3a8a0211ddc944c3829df023b285509b |
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| 出典メモ | uspto-grants-2011_12 |
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