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HRID 376961作成日:2026年10月27日

1,3-Propanedithiol → 1-[4-(3-Mercaptopropylthio)phenyl]-2-dimethylamino-2-benzyl-butan-1-one

https://huagongshe.com/reaction/376961

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-PropanedithiolHCID 8013—
反応物Potassium CarbonateHCID 11430—
反応物2-Benzyl-2-(dimethylamino)-1-(4-fluorophenyl)butan-1-oneHCID 19360599—
溶媒DimethylacetamideHCID 31374—
生成物1-[4-(3-Mercaptopropylthio)phenyl]-2-dimethylamino-2-benzyl-butan-1-oneHCID 19360633—

反応条件

温度50 °C

反応手順

32.5 g (0.3 mol) of 1,3-propanedithiol are dissolved in 50 ml of dry dimethylacetamide, and the solution is heated to about 50° C. together with 13.8 g (0.1 mol) of potassium carbonate. 15.0 g (0.05 mol) of 1-(4-fluorophenyl)-2-dimethylamino-2-benzyl-butan-1-one in 30 ml of dry dimethylacetamide are added dropwise. The suspension is stirred at 50° C. overnight (about 12 hours), then the solid is filtered off. The excess 1,3-propanedithiol and dimethylacetamide are distilled off. To the residue is added toluene, then the precipitate is filtered off. After distilling off the toluene, the residue is purified by means of column chromatography on silica gel with ethyl acetate-hexane (1:7) as an eluent, and an oily product is obtained. The structure is confirmed by the 1H-NMR spectrum (CDCl3): δ [ppm]: 0.68 (t, 3H), 1.39 (t, 1H), 1.79-1.88 (m, 1H), 1.97-2.11 (m, 3H), 2.36 (s, 6H), 2.69 (q, 2H), 3.12 (t, 2H), 3.19 (s, 2H), 7.15-7.27 (m, 7H), 8.28 (d, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06022906
出典データセットuspto-grants-2000_02
ORD IDord-cab446e251fe4108813cf01645b94b33
出典メモuspto-grants-2000_02