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HRID 2213663作成日:2026年10月25日
tert-Butyl 2-formyl-1H-pyrrole-1-carboxylate → [N-(dimethylethoxycarbonyl)pyrrol-2-yl](3-aminophenyl)methanol
https://huagongshe.com/reaction/2213663
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | tert-Butyl 2-formyl-1H-pyrrole-1-carboxylate | HCID 5057005 | — |
| 反応物 | HCID 178504299 | HCID 178504299 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | [N-(dimethylethoxycarbonyl)pyrrol-2-yl](3-aminophenyl)methanol | HCID 21957618 | — |
反応手順
A solution of N-(dimethylethoxycarbonyl)pyrrole-2-carboxaldehyde (10 g, 50 mmol) in THF (500 mL) at −30° C. under nitrogen was added dropwise to 3-[bis(trimethylsilyl)amino]phenylmagnesium chloride (55 mL of a 1M solution in THF, 55 mmol). After addition the reaction mixture was gradually warmed up and stirred at 0° C. for 1 hour, then at ambient temperature for 15 minutes. The reaction mixture was poured into ice water, and stirred for 30 minutes. The reaction mixture was extracted with ethyl ether (1 L). The combined organic layers were dried (Na2SO4) and concentrated. Chromatography on SiO2 (700 g) using 1:1 hexane/ethyl acetate afforded [N-(dimethylethoxycarbonyl)pyrrol-2-yl](3-aminophenyl)methanol (11.2 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07105563B2 |
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| 出典データセット | uspto-grants-2006_09 |
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| ORD ID | ord-4522992528e14ea8babc3e79fad1260f |
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| 出典メモ | uspto-grants-2006_09 |
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