戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 840233作成日:2026年10月26日

Acetone → 3-(Benzo[1,3]dioxol-5-ylamino)-2-(2,2-dimethyl-propionyl)-3-methylsulfanyl-propenenitrile

https://huagongshe.com/reaction/840233

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Methyl iodideHCID 6328—
反応物Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
反応物1,3-Benzodioxole, 5-isothiocyanato-HCID 123593—
生成物3-(Benzo[1,3]dioxol-5-ylamino)-2-(2,2-dimethyl-propionyl)-3-methylsulfanyl-propenenitrileHCID 7015092698%

反応手順

To a solution of 4,4-dimethyl-3-oxopentanenitrile (0.626 g, 5.0 mmol) in dry acetone (10 ml) first potassium carbonate (1.38 g, 10 mmol) and then 3,4-methylendioxyphenyl isothiocyanate (0.941 g, 5.3 mmol) were added. The resulting mixture was stirred at room temperature under nitrogen for 72 h, and then filtered. To the filtrate methyl iodide (0.93 ml, 15 mmol) was added. The mixture was stirred at room temperature for 45 min. The precipitate was filtered off and the filtrate was concentrated. The residue was taken up into dichloromethane and water. The organic layer was washed with water (2×), dried (sodium sulfate) and concentrated. Crystallisation from ethyl acetate/heptane 1:1 gave 1.56 g (98%) of the title compound. Mp 139-141° C.; 1H NMR (200 MHz, CDCl3): δ=1.40 (s, 9H), 2.28 (s, 3H), 6.03 (s, 2H), 6.75 (dd, 1H), 6.8 (m, 2H), 13.5 (br s, 1H); EI SP/MS: 318 (M+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06365609B1
出典データセットuspto-grants-2002_04
ORD IDord-2d293ca67fa640d18060d813dce05ab2
出典メモuspto-grants-2002_04