Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063936Generated: October 26, 2026

3,4-dihydro-2H-pyran → 4-Chloro-2-nitro-1-[[(tetrahydro-2H-pyran-2-yl)oxy]methyl]benzene

https://huagongshe.com/reaction/1063936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant4-Chloro-2-nitrobenzyl alcoholHCID 89956—
ReactantPyridiniumHCID 4989215—
CatalystToluenesulfonateHCID 3424274—
SolventDichloromethaneHCID 6344—
Product4-Chloro-2-nitro-1-[[(tetrahydro-2H-pyran-2-yl)oxy]methyl]benzeneHCID 2227621562.3%

Reaction Steps

A magnetically stirred solution of 4-chloro-2-nitrobenzyl alcohol (25.0 g, 133 mmol) and 3,4-dihydro-2H-pyran (118.2 mL, 16.8 g, 200 mol) in anhydrous dichloromethane (250 mL) was treated at 25° C. with pyridinium (toluenesulfonate (PPTS, 50 mg). The solution was stirred for 12 h, washed with 1 N NaOH (250 mL), brine (250 mL), dried (K2CO3), filtered, and concentrated in vacuo. Silica gel chromatography (4:1 hexane:ethyl acetate) of the concentrate gave 22.5 g (62%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967196B1
Source datasetuspto-grants-2005_11
ORD IDord-476e4a958f394232a507765528dae39f
Source noteuspto-grants-2005_11