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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910704Generated: October 28, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 2,4-Dichloro-6-(3-chloro-thiophen-2-yl)-pyrimidine

https://huagongshe.com/reaction/910704

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant2,4-DichloropyrimidineHCID 77531—
Reactant3-ChlorothiopheneHCID 87017—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2,4-Dichloro-6-(3-chloro-thiophen-2-yl)-pyrimidineHCID 86628639—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-chlorothiophene (384 mg, 3.0 mmol) in THF (6 mL) at −78° C. was added n-BuLi (1.6 M, 2 mL) and the resulting mixture stirred for 45 minutes. The resulting product was added to a solution of 2,4-dichloropyrimidine (430 mg, 2.9 mmol) in ether (10 mL) at −30° C. and the resulting mixture stirred for 30 minutes, then warmed up to 0° C. and stirred for another 30 minutes. DDQ (700 mg, 3 mmol) was added and the resulting mixture was stirred overnight, then filtered through Celite®. The filtrate was concentrated and the residue was purified by silica gel column (EtOAc/hexanes, 1:5) to yield a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022209B2
Source datasetuspto-grants-2011_09
ORD IDord-27539537da2646b39a7265817ece70a2
Source noteuspto-grants-2011_09