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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989100Generated: October 25, 2026

Ammonium Chloride → 2-Chloro-4-(4-chlorophenyl)-6-cyclopropylpyrimidine

https://huagongshe.com/reaction/1989100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantPyrimidine, 2,4-dichloro-6-(4-chlorophenyl)-HCID 11623053—
ReactantHCID 178420628HCID 178420628—
ReactantHCID 178420684HCID 178420684—
Catalystzinc chloride THFHCID 66790640—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-4-(4-chlorophenyl)-6-cyclopropylpyrimidineHCID 5746861642%

Reaction Steps

To a solution of 2,4-dichloro-6-(4-chloro-phenyl)-pyrimidine (2.6 g, 10.0 mmol) and tetrakis(triphenylphosphine)palladium (0.69 g, 0.6 mmol) in THF (10 mL) was added at 20° C. a 0.25 M cyclopropylzinc chloride/THF solution (120 mL, 30 mmol; freshly prepared by stirring a mixture of 60 mL of 0.5 M cyclopropylmagnesium bromide/THF and 60 mL of 0.5 M zinc chloride/THF for 1 h at 0° C., followed by 1 h at 20° C.) and the mixture was refluxed in an atmosphere of argon for 3 h. After the slow addition of sat. aqueous NH4Cl solution (20 mL) at 0° C. the mixture was partitioned between AcOEt and 10% sodium chloride solution. The organic layer was dried (Na2SO4) and evaporated in vacuo. The residue was chromatographed on silica gel using AcOEt/cyclohexane (1:19 v/v) as eluent to give 2-chloro-4-(4-chloro-phenyl)-6-cyclopropyl-pyrimidine (1.12 g, 42%) as a light yellow solid. MS (ISP) 265.1 [(M+H)+]; mp 70-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642264B2
Source datasetuspto-grants-2010_01
ORD IDord-809fb29b9f34454b8b77b38bf9a65c40
Source noteuspto-grants-2010_01