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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171673Generated: October 31, 2026

Tetrahydrofuran → HCID 63867842, compound

https://huagongshe.com/reaction/2171673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantTetrahydro-4H-pyran-4-olHCID 74956—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 63867842HCID 6386784271.1%

Reaction Steps

Tetrahydro-2H-pyran-4-ol (200 mg) was mixed with THF (5 ml), and sodium hydride (55% suspended in oil) (120 mg) was added thereto, followed by stirring at room temperature for 5 minutes. 5-Bromo-2-chloropyrimidine (460 mg) was added to the reaction mixture, followed by stirring at room temperature. Water and EtOAc were added to the reaction mixture, and the organic layer was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/EtOAc) to obtain 5-bromo-2-(tetrahydro-2H-pyran-4-yloxy)pyrimidine (361 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051283B2
Source datasetuspto-grants-2015_06
ORD IDord-8636ff26fa874297ab94f43b2c56585a
Source noteuspto-grants-2015_06