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HRID 21850作成日:2026年10月25日

1,2-Dichloroethane → 2-Methyl-4-(1-oxopropoxy)-2-butenal

https://huagongshe.com/reaction/21850

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物HexamethylenetetramineHCID 4101—
反応物TetramethylenedisulfotetramineHCID 64148—
反応物4-Propionyloxy-2-methyl-1-chloro-2-buteneHCID 53656894—
溶媒WaterHCID 962—
生成物2-Methyl-4-(1-oxopropoxy)-2-butenalHCID 5723975226.8%

反応条件

温度35 °C

反応手順

The crude 4-propionyloxy-2-methyl-1-chloro-2-butene (64.0 g, 0.362 mol) obtained in the above (i) was added to a solution of hexamethylenetetramine (50.9 g, 0.363 mol) in water (345 ml), and the mixture was stirred at 35° C. for 4 hours to prepare a tetramine salt. 1,2-Dichloroethane (200 ml) was added to the reaction mixture, and compounds insoluble in water were removed by extraction. 1,2-Dichloroethane (400 ml) was further added to the aqueous layer that had been washed, and the mixture was stirred at 60° C. for 4 hours to hydrolyze the tetramine salt. After completion of the reaction, the 1,2-dichloroethane layer was separated, and 1,2-dichloroethane (250 ml) was further added to the aqueous layer for extraction. The 1,2-dichloroethane layers were combined and dried over anhydrous sodium sulfate. The 1,2-dichloroethane was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate-hexane (=1:5)) to give 4-propionyloxy-2-methyl-2-buten-1-al (15.2 g, 0.0973 mol, Yield: 26.8% ).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05424478
出典データセットuspto-grants-1995_06
ORD IDord-058f1754f95a4ac2af5d634a51172185
出典メモuspto-grants-1995_06