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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822773Generated: November 1, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 4,6-Dichloro-2-ethenylpyrimidine

https://huagongshe.com/reaction/1822773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantTetravinylstannaneHCID 66189—
Reactant4,6-DichloropyrimidineHCID 70943—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178506890HCID 178506890—
SolventDiethyl EtherHCID 3283—
Product4,6-Dichloro-2-ethenylpyrimidineHCID 22170034—

Reaction Conditions

Temperature0 °C

Reaction Steps

Vinyl lithium (10 mmol; generated from the reaction of nBuLi with tetravinyltin in diethyl ether) was added to a solution of 4,6-dichloropyrimidine (1.49 g, 10 mmol) in diethyl ether (70 mL) under an argon atmosphere at −30° C. The reaction mixture was quenched with acetic acid (600 mL) and water (200 mL) after stirring for 60 min. DDQ (2.27 g, 10 mmol) was added and the reaction mixture was warmed to 0° C. and stirred for 2 hr. The brownish slurry was then washed three times with 1M NaOH, once with brine and dried over MgSO4. Filtration followed by removal of volatiles under reduced pressure afforded a dark brown tar from which 2-vinyl-4,6-dichloropyrimidine was isolated by flash chromatography (10% ethyl acetate in hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037916B2
Source datasetuspto-grants-2006_05
ORD IDord-67c0756073e1490d89fdeeb67837a60e
Source noteuspto-grants-2006_05