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1-Naphthaldehyde → Methyl (2-(1-naphthyl)-6-benzoxazolyl)acetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Naphthaldehyde | HCID 6195 | — |
| 反応物 | Iodo benzene diacetate | HCID 12217721 | — |
| 反応物 | Methyl 2-(4-amino-3-hydroxyphenyl)acetate | HCID 17858854 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Methyl (2-(1-naphthyl)-6-benzoxazolyl)acetate | HCID 58778440 | 42% |
反応手順
In EtOH (8 ml), 1-naphthaldehyde (263 mg, 1.68 mmol) and methyl 4-amino-3-hydroxyphenylacetate (305 mg, 1.68 mmol) were stirred at room temperature for 12 hours. Iodobenzene diacetate (651 mg, 2.02 mmol) was added to the reaction mixture, followed by stirring at room temperature for 5 minutes. After removal of the solvent by distilling the reaction mixture under reduced pressure, the residue was purified by chromatography on a silica gel column, whereby from n-hexane/ethyl acetate (6:1, v/v) eluate fractions, methyl (2-(1-naphthyl)-6-benzoxazolyl)acetate (223 mg, 42%) was obtained as a pale yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07157487B2 |
| 出典データセット | uspto-grants-2007_01 |
| ORD ID | ord-90e088c89fe94f72af7c19ed60ce651e |
| 出典メモ | uspto-grants-2007_01 |