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HRID 862941作成日:2026年10月25日
2-Bromoanisole → Ethyl (1RS) 1-Hydroxy-1-(methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indene-2-carboxylate
https://huagongshe.com/reaction/862941
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Bromoanisole | HCID 11358 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 反応物 | Ethyl 3-(3,4-methylenedioxyphenyl)1-oxoindene-2-carboxylate | HCID 18427631 | — |
| 反応物 | HCID 178489560 | HCID 178489560 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Ethyl (1RS) 1-Hydroxy-1-(methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indene-2-carboxylate | HCID 18969641 | — |
反応手順
To dry magnesium turnings (81 mg, 3,4 mmol) under an argon atmosphere was added a solution of 2-bromoanisole (0.64 g, 3,4 mmol) in 5:1 THF/Et2 O (3 ml). A portion of the resulting 2-methoxyphenyl magnesium bromide solution (0.45 ml, 0.51 mmol) was added dropwise to a solution of ethyl 3-(3,4-methylenedioxyphenyl)-1-oxoindene-2-carboxylate (100 mg, 0.34 mmol) in THF (6 ml) under an argon atmosphere at 0° C. After stirring for 15 min, the mixture was partitioned between 3M HCl and EtOAc. The organic extract was washed successively with H2O, 5% aqueous NaHCO3, H2O and saturated aqueous NaCl. The solvent was removed in vacuo, and the residue was purified by flash chromatography, eluting with 15% EtOAc/hexanes to afford the title compound. (100 mg, 68%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05719182 |
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| 出典データセット | uspto-grants-1998_02 |
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| ORD ID | ord-e45b0f6257fa4ccea14365a2a0cc8419 |
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| 出典メモ | uspto-grants-1998_02 |
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