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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462857Generated: October 26, 2026

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

https://huagongshe.com/reaction/1462857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantThiophene, 2,5-dihydro-3-methyl-, 1,1-dioxideHCID 70941—
SolventDiethyl EtherHCID 3283—
ProductThiophene, 3-(bromomethyl)-2,5-dihydro-, 1,1-dioxideHCID 71295834.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04461764
Source datasetuspto-grants-1984_07
ORD IDord-4ee0407e9047430eacd01aa33f279a11
Source noteuspto-grants-1984_07