Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646438Generated: November 2, 2026

Chloroform → HCID 19800635, compound

https://huagongshe.com/reaction/1646438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant3-VINYLTHIOPHENEHCID 10887853—
ReactantHCID 13730721HCID 13730721—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 19800635HCID 19800635—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 3-vinylthiophene (10.0 g, 0.0908 mol), α-isopropyl-α-methyl-2,5-dioxo-3-pyrroline-1- acetonitrile (18.3 g, 0.0953 mol) and chloroform is stirred at 50° C. for 20 hours and at room temperature for one week. The mixture is concentrated in vacuo to give a yellow oil residue, which is column chromatographed on silica gel using methylene chloride as an eluent to afford a yellow oil. The oil is taken up in dioxane and treated with dichlorodicyano-p-benzoquinone, (17.2 g, 0.0760 mol), stirred for 21 hours at 100° C., cooled to 25° C. and filtered (the filter cake is washed once with benzene). The filtrate is concentrated in vacuo to give an orange semisolid residue. The residue is washed through neutral alumina with methylene chloride:hexanes (1:1) and flash chromatographed on silica gel using hexane:ethyl acetate (4:1) as an eluent to afford the title product as a pale yellow solid, 4.21 g (15.6%), mp 99°-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180419
Source datasetuspto-grants-1993_01
ORD IDord-c6a0e982524841f99b497ffbb27e96d3
Source noteuspto-grants-1993_01