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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989131Generated: November 2, 2026

3,4-dihydro-2H-pyran → 2-Bromo-6-(tetrahydro-pyran-2-yloxymethyl)-4-(4-trifluoromethyl-phenyl)-pyridine

https://huagongshe.com/reaction/1989131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantEthylacetate heptaneHCID 21899848—
Reactant[6-Bromo-4-(4-trifluoromethyl-phenyl)-pyridin-2-yl]-methanolHCID 60209333—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventDichloromethaneHCID 6344—
Product2-Bromo-6-(tetrahydro-pyran-2-yloxymethyl)-4-(4-trifluoromethyl-phenyl)-pyridineHCID 5746869887.2%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of the above described [6-bromo-4-(4-trifluoromethyl-phenyl)-pyridin-2-yl]-methanol (4.2 g, 95%, purity 81%) and 3,4-dihydro-2H-pyran (1.4 ml, 15.4 mmol) in DCM (20 ml) at 23° C. was added a catalytic amount of p-TsOH.H2O (10 mg) and the mixture was stirred at 23° C. for 18 h. Then again 3,4-dihydro-2H-pyran (0.7 ml, 7.68 mmol) was added and stirring was continued at 23° C. for another 2 h. The entire reaction mixture was directly subjected to silica gel column chromatography with n-heptane/AcOEt to give the title compound (4.59 g, 100%, 93% purity) as a light yellow oil. MS (ISP) 418.2 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642264B2
Source datasetuspto-grants-2010_01
ORD IDord-770d8dd8f9274c1b9630043dbe579e66
Source noteuspto-grants-2010_01