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Triethylamine → 4-Iodo-3-(naphthalen-2-yloxy)-benzoic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 3-Hydroxy-4-iodobenzoic acid | HCID 736854 | — |
| 反応物 | (Naphthalen-2-yl)boronic acid | HCID 2734375 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-Iodo-3-(naphthalen-2-yloxy)-benzoic acid methyl ester | HCID 53921157 | — |
反応手順
A mixture of 3-hydroxy-4-iodo-benzoic acid acid methyl ester (0.505 g, 1.82 mmol), cupric acetate (0.330 g, 1.82 mmol), 2-naphthylboronic acid (0.625 g, 3.63 mmol) and powdered 4A molecular sieves (0.3 g) in CH2Cl2 (21 mL) was treated with triethylamine (1.27 mL, 9.08 mmol) and stirred at ambient temperature for 18 hr. The reaction mixture was filtered through celite, concentrated to dryness and chromatographed (SiO2, 5-40% EtOAc: hexane) to give the title compound. FAB mass spectrum (M+1) 405.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06297239B1 |
| 出典データセット | uspto-grants-2001_10 |
| ORD ID | ord-4c3bea01e7014b94b4af9526bf27f2c4 |
| 出典メモ | uspto-grants-2001_10 |