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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363882Generated: October 29, 2026

2,6-Dichlorophenol → HCID 86605407, compound

https://huagongshe.com/reaction/1363882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichlorophenolHCID 6899—
Reactant2,4,6-TrichloropyrimidineHCID 77378—
ReactantPotassium hydroxide ethanolHCID 21946426—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86605407HCID 8660540755.1%

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-(2,6-dichlorophenoxy)pyrimidine (55%) (interm. 12).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07887845B2
Source datasetuspto-grants-2011_02
ORD IDord-e6d7b0588cfc42389c0f04d1b2aa0177
Source noteuspto-grants-2011_02