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HRID 19528作成日:2026年10月26日
Ethyl 6-methoxy-1-oxo-3-phenyl-1H-indene-2-carboxylate → 1-cyclohexyl-1-hydroxy-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/19528
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl 6-methoxy-1-oxo-3-phenyl-1H-indene-2-carboxylate | HCID 23249734 | — |
| 反応物 | HCID 178478990 | HCID 178478990 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-cyclohexyl-1-hydroxy-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl ester | HCID 11639752 | 30.2% |
反応手順
6-Methoxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid ethyl ester (78 mg, 0.253 mmol) obtained in Example 1 was dissolved in THF, and 18%-cyclohexylmagnesium chloride (0.7 mL, 0.506 mmol) was added thereto, followed by stirring for 5 hrs at 0° C. The resulting mixture washed with saturated saline and extracted with ethyl acetate. The organic layer was separated, dried over anhydrous MgSO4, and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 30 mg of the titled compound (yield: 30%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07745439B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-7a10624842704a7abc2067372af0646d |
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| 出典メモ | uspto-grants-2010_06 |
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