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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070943Generated: October 29, 2026

2,6-Dichlorophenol → HCID 22398418, compound

https://huagongshe.com/reaction/1070943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichlorophenolHCID 6899—
Reactant2,4,6-TrichloropyrimidineHCID 77378—
ReactantPotassium hydroxide ethanolHCID 21946426—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22398418HCID 2239841855.1%

Reaction Steps

Potassium hydroxide/ethanol (10%; 0.035 mol) was added to a solution of 2,6-dichlorophenol (0.035 mol) in tetrahydrofuran (100 ml). The mixture was stirred and 2,4,6-trichloropyrimidine (0.044 mol) was added. The mixture was stirred overnight at 60° C. The reaction was quenched with NaOH 1N solution. The aqueous layers were extracted with EtOAc several times and then the organic layers were combined and washed with NaOH 3N and saturated NaCl, dried and concentrated. The residue was recrystallized from CH2Cl2/hexane. The precipitate was filtered off and dried, yielding 5.98 g 2,4-dichloro-6-(2,6-dichlorophenoxy)pyrimidine (55%) (interm. 12).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903213B2
Source datasetuspto-grants-2005_06
ORD IDord-0434ae91dea34667b77a3971816373ff
Source noteuspto-grants-2005_06