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HRID 1661861作成日:2026年10月24日

4-Acetylbutyric acid → Pentafluorophenyl 5-oxohexanoate

https://huagongshe.com/ja/reaction/1661861

反応式

関与物質

役割名称HCID仕込み量
反応物4-Acetylbutyric acidHCID 18407—
反応物DiisopropylethylamineHCID 81531—
反応物Pentafluorophenyl TrifluoroacetateHCID 4327891—
溶媒DichloromethaneHCID 6344—
生成物Pentafluorophenyl 5-oxohexanoateHCID 8660918979.3%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08030460B2
出典データセットuspto-grants-2011_10
ORD IDord-2198ed722c8541519be28b40df71a586
出典メモuspto-grants-2011_10