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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637794Generated: November 2, 2026

3,4-Dichlorophenol → HCID 13560225, compound

https://huagongshe.com/reaction/637794

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichlorophenolHCID 7258—
ReactantHCID 13560204HCID 13560204—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13560225HCID 1356022554%

Reaction Steps

Following a procedure substantially the same as that described in Example 20, 8.0 g of 3-chloro-6-ethylthio-2-pyridinecarbonitrile was reacted with 8.2 g of 3,4-dichlorophenol in the presence of 5.6 g of t-BuOK in 60 ml of THF and 30 ml of DMSO. The reaction was allowed to proceed at boiling temperature for about 40 hours. The product, an oil, was purified by distillation on a Kugelrohr distillation apparatus, separated on a Water's Prep LC 500 instrument, and again distilled on a Kugelrohr apparatus to give about 7 g (54%) of the desired 3-(3,4-dichlorophenoxy)-6-ethylthio-2-pyridinecarbonitrile, having a boiling point (b.p.) of 160° C. at 0.01 mm Hg pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04558134
Source datasetuspto-grants-1985_12
ORD IDord-e357cdff050549c98738fa1824272f4e
Source noteuspto-grants-1985_12