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HRID 583638作成日:2026年10月26日

Propanal → 2-Methyl-4-(2,2,3-trimethylcyclopent-3-enyl)pent-2-enal

https://huagongshe.com/reaction/583638

反応式

関与物質

役割名称HCID仕込み量
反応物PropanalHCID 527—
反応物3-Cyclopentene-1-acetaldehyde, 2,2,3-trimethyl-HCID 98497—
反応物SodiumHCID 5360545—
反応物2-(2,2,3-Trimethylcyclopent-3-enyl)propionaldehydeHCID 10352057—
反応物Sodium MethoxideHCID 10942334—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物2-Methyl-4-(2,2,3-trimethylcyclopent-3-enyl)pent-2-enalHCID 5727975938%

反応条件

温度10 °C

反応手順

60.0 g (0.36 mol) of 2-(2,2,3-trimethylcyclopent-3-enyl)propionaldehyde, prepared from campholenic aldehyde as known per se, and 42.0 g (0.72 mol) of propanal was added successively during 15 min and 2 hours, respectively, to the sodium methylate solution prepared from 0.83 g of sodium and 200 ml of anhydrous methanol, at 10° C. The reaction mixture was stirred at 10° C. for 2 hours and at room temperature for the following 42 hours. After addition of 5 ml of acetic acid the solvent was evaporated in vacuo at the temperature maintained below 50° C. The residue was diluted with 500 ml of MTBE, washed with 2×200 ml of brine, dried (MgSO4), concentrated in vacuo and distilled at 76-95° C./0.1 Torr to give 28.1 g (38%) of 2-methyl-4-(2,2,3-trimethylcyclopent-3-enyl)pent-2-enal. An analytical sample was prepared by flash chromatography on silica gel (eluent: hexane/MTBE 12:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05929291
出典データセットuspto-grants-1999_07
ORD IDord-e0ca7fa447224dd894004f9708336f3f
出典メモuspto-grants-1999_07