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Triethylamine → (E)-ethyl 3-(3-((methoxymethoxy)methyl)phenyl)acrylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Ethyl Acrylate | HCID 8821 | — |
| 反応物 | Tri-o-tolylphosphine | HCID 80271 | — |
| 反応物 | 1-Bromo-3-[(methoxymethoxy)methyl]benzene | HCID 11447578 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (E)-ethyl 3-(3-((methoxymethoxy)methyl)phenyl)acrylate | HCID 131736029 | — |
反応手順
Under a nitrogen atmosphere, a crude product of 1-bromo-3-((methoxymethoxy)methyl)benzene (3.60 g), triethylamine (6.50 mL), palladium acetate (175 mg), tri-o-tolylphosphine (711 mg) and ethyl acrylate (8.4 mL) were stirred in DMF (30 mL) at 110° C. for 1 hr. The solvent of the reaction mixture was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (NH, ethyl acetate/hexane) to give the title compound (3.41 g) as a pale-yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09382188B2 |
| 出典データセット | uspto-grants-2016_07 |
| ORD ID | ord-cea30461553949a49694e8212e9a80e1 |
| 出典メモ | uspto-grants-2016_07 |