戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2235821作成日:2026年10月25日

Isopropanol → 1,3-Diphenylpentane-1,4-dione

https://huagongshe.com/reaction/2235821

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物CinnamoylbenzeneHCID 7189—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物AcetyltrimethylsilaneHCID 638116—
触媒3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromideHCID 9964923—
溶媒TetrahydrofuranHCID 8028—
生成物1,3-Diphenylpentane-1,4-dioneHCID 13184731—

反応条件

温度70 °C

反応手順

1-Trimethylsilanyl-ethanone (1.15 mL; 8.02 mmol) followed by DBU (0.18 mL; 1.2 mmol) were added to a suspension of 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide (304 mg; 1.21 mmol) in dry THF (5 mL). The mixture was heated at 70° C. for 4 min, cooled near rt, then chalcone (833 mg; 4.00 mmol) and 2-propanol (1.22 mL; 15.9 mmol) were added. The reaction was degassed and reacted under nitrogen at 70° C. After 24 h, the reaction was concentrated on a rotary evaporator. Ethyl acetate (25 mL) was added and this washed with H2O (3×3 mL) and satd NaCl (2×3 mL). The organic portion was dried (MgSO4) and filtered through silica with an EtOAc wash. Crude product was adsorbed onto silica (2 g) then purified by MPLC (40 g of silica using a 0→20% EtOAc in hexanes gradient). Pure product was obtained as a clear, colorless viscous liquid (980 mg; 97%). 1H NMR (CDCl3) δ 7.98-7.94 (m, 2H), 7.56 (m, 1H), 7.47-7.42 (m, 2H), 7.39-7.27 (m, 5H), 4.44 (dd, J=3.6, 10.0 Hz, 1H), 4.02 (dd, J=10.0, 18.0 Hz, 1H), 3.14 (dd, J=3.6, 18.0 Hz, 1H); GC-MS 252 ([M]+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07714022B2
出典データセットuspto-grants-2010_05
ORD IDord-2b415d0225974738b2789e274fe179f6
出典メモuspto-grants-2010_05