化工社化工社 化学情報印刷レポート · 研究参考用
4-Acetylbutyric acid → Pentafluorophenyl 5-oxohexanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Acetylbutyric acid | HCID 18407 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Pentafluorophenyl Trifluoroacetate | HCID 4327891 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Pentafluorophenyl 5-oxohexanoate | HCID 86609189 | 79.3% |
反応手順
5-Oxohexanoic acid (2.6 g; 20 mmol) was dissolved in CH2Cl2 (50 mL). N,N-Diisopropylethylamine (10.4 mL, 60 mmol) was added followed by pentafluorophenyl trifluoroacetate (3.61 mL; 21 mmol). The reaction mixture was kept at room temperature for 1 hour and evaporated. The residue was resuspended in EtOAc:Hexanes (1:1) and loaded on a silica gel column (5×20 cm) equilibrated and developed with the same mixture. Fractions containing the product (14) (Rf ˜0.7) were pooled and concentrated to give 4.7 g (79%) of yellowish oil after drying in vacuum. 1H NMR (CDCl3) δ 2.05 (m, 2H), 2.18 (s, 3H), 2.61 (t, 2H), 2.74 (t, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08030460B2 |
| 出典データセット | uspto-grants-2011_10 |
| ORD ID | ord-2198ed722c8541519be28b40df71a586 |
| 出典メモ | uspto-grants-2011_10 |