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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22943Generated: October 27, 2026

Sodium hydride → HCID 178511712, compound

https://huagongshe.com/reaction/22943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-ChloropyrimidineHCID 74404—
ReactantHCID 178479278HCID 178479278—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178511712HCID 178511712—

Reaction Steps

60% sodium hydride was added to 10 ml of a tetrahydrofuran suspension containing 1.00 g of trans-4-aminocyclohexanol hydrochloride and the mixture was refluxed for 1 hour. After cooling to room temperature, 2-chloropyrimidine was slowly added thereto and the mixture was stirred at room temperature for 6 hours. The reaction mixture was poured into ice-cold water and extracted with chloroform. The extract was washed with brine and dried over anhydrous sodium sulfate, and then, the solvent was removed under reduced pressure. The residue was purified by NH-silica gel column chromatography (solvent: ethyl acetate-hexane (1:4) to chloroform alone) to obtain 788 mg of trans-4-(2-pyrimidinyloxy)cyclohexylamine (Reference Example 9-46 in Table 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849622B2
Source datasetuspto-grants-2005_02
ORD IDord-177949fd58514cb08143173f2492b15a
Source noteuspto-grants-2005_02