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HRID 1462857作成日:2026年10月27日

Chloroform → Thiophene, 3-(bromomethyl)-2,5-dihydro-, 1,1-dioxide

https://huagongshe.com/reaction/1462857

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroformHCID 6212—
反応物Benzoyl PeroxideHCID 7187—
反応物N-bromobutanimideHCID 67184—
反応物Thiophene, 2,5-dihydro-3-methyl-, 1,1-dioxideHCID 70941—
溶媒Diethyl EtherHCID 3283—
生成物Thiophene, 3-(bromomethyl)-2,5-dihydro-, 1,1-dioxideHCID 71295834.2%

反応条件

温度0 °C

反応手順

In a reaction vessel, 21.0 gms (0.1591 moles) 3-methyl sulfolene, 28.32 gms (0.1591 moles) N-bromo succinimide, 1.9 gms (0.0008 moles) benzoyl peroxide and 250 ml chlorform were combined. The resulting mixture was heated to reflux and then refluxed for 20 hours. The reaction mixture was cooled to 0° C. and then filtered to remove the succinimide. The filtrate was stripped until only a small amount of solvent remained. The remaining solids were removed by filtration, and the remainder of the solvent was stripped to give an orange oil. Ether was added to the oil. After a few minutes, the solids crystallized. Filtration and drying yielded 11.5 gms of the product. The NMR and IR spectra confirmed the structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04461764
出典データセットuspto-grants-1984_07
ORD IDord-4ee0407e9047430eacd01aa33f279a11
出典メモuspto-grants-1984_07