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HRID 70756作成日:2026年10月25日

2,3-Dimethoxy-1,3-butadiene → 3,4-Dimethoxyselenophene

https://huagongshe.com/reaction/70756

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-Dimethoxy-1,3-butadieneHCID 19169—
反応物Selenium chlorideHCID 139762—
反応物Acetone cardiceHCID 18522661—
反応物HCID 178418247HCID 178418247—
溶媒HexaneHCID 8058—
生成物3,4-DimethoxyselenopheneHCID 24886169—

反応条件

温度-78 °C

反応手順

To a well stirred solution of 2,3-dimethoxy-1,3-butadiene (1.47 g, 12.9 mmol, (11)) and CH3COONa (2.64 g, 32.25 mmol) in dry hexane (80 mL) at −78° C. (dry ice/acetone bath), under an inert atmosphere, was added a solution of freshly prepared SeCl2 in hexane over a period of 15 min. The resulting yellowish solution was further stirred for 1 h at −78° C. and then removed from the cooling bath and the reaction mixture was brought to room temperature over a period of 2 h and further stirred for 5 h. The reaction mixture was filtered through neutral alumina and washed with hexane. The residue was concentrated to give brown yellow oil. The crude product was purified by flash column chromatography on TLC grade silica gel (Hexane:Ethyl acetate—95:5) to provide DMOS (0.85 g, 35%, (12)) as a white crystalline solid. mp. 43-45° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822635B2
出典データセットuspto-grants-2014_09
ORD IDord-18f9441165df4406b6d2489b4d5df025
出典メモuspto-grants-2014_09