関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl diazoacetate | HCID 12192 | — |
| 反応物 | 1-(p-Bromobenzyl)-5-methoxy-2-methyl-3-vinylindole | HCID 19974943 | — |
| 触媒 | Rhodium(II) Octanoate Dimer | HCID 6099591 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Ethyl 2-[1-(p-bromobenzyl)-5-methoxy-2-methylindol-3-yl]cyclopropanecarboxylate | HCID 19974929 | — |
反応手順
To a room temperature solution of the indole from Step 1 (3.91 g, 11.0 mmol) in 20 mL toluene was added rhodium (II) octanoate dimer (109 mg, 0.14 mmol), and the solution was cooled to 0° C. A solution of ethyl diazoacetate (3.0 mL, 28.5 mmol) in 13 mL toluene was then added via syringe pump at 1.2 mL/hr. Fresh catalyst was then added along with an additional 1 mL ethyl diazoacetate in toluene over 2.5 h. The crude reaction mixture was applied directly to a silica gel column and eluted with 1% to 2.5% ethyl acetate/toluene. 1.1 g of the trans isomer of the title compound was thus obtained, followed by 1.2 g of the cis isomer of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05604253 |
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| 出典データセット | uspto-grants-1997_02 |
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| ORD ID | ord-ee257a9407da4a4ea70b259c601b9e2e |
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| 出典メモ | uspto-grants-1997_02 |
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