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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | Tetravinylstannane | HCID 66189 | — |
| Reactant | 4,6-Dichloropyrimidine | HCID 70943 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178506890 | HCID 178506890 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4,6-Dichloro-2-ethenylpyrimidine | HCID 22170034 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07037916B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-67c0756073e1490d89fdeeb67837a60e |
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| Source note | uspto-grants-2006_05 |
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