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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059577Generated: October 30, 2026

Pyridine → HCID 59226230, compound

https://huagongshe.com/reaction/2059577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 59226238HCID 59226238—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventPyridine methylene chlorideHCID 21875418—
ProductHCID 59226230HCID 5922623065%

Reaction Steps

147.0 g (3-Chloro-4-fluoro-benzyl)-(2,2-dimethoxy-ethyl)-amine (1, crude product) were dissolved in 540 ml of dichloromethane/pyridine (8:1). At 0° C. a solution of 145.8 g (1.04 mol) p-toluenesulfonylchloride in 200 ml of dichloromethane was added. After 5 h at room temperature additional 20 ml of pyridine, 29.16 g (0.15 mol) p-toluene-sulfonylchloride and a catalytic amount of DMAP were added. The solution was stirred at room temperature for 7 h and then refluxed for additional 4 h. Again 29.16 g (0.15 mol) p-toluene-sulfonylchloride and a catalytic amount of DMAP were added and the mixture was stirred overnight. For workup, the solution was washed twice with 2 N HCl and twice with saturated NaHCO3-solution. The organic layer was dried with MgSO4 and evaporated. Final silica gel chromatography (heptane/ethyl acetate 4:1) gave 155 g of the title compound as a yellow oil. Rt=1.80 min (Method B). Detected mass: 370.2 (M-OMe−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278294B2
Source datasetuspto-grants-2012_10
ORD IDord-c154f87b40e54512916f4e6e3a9ad8e1
Source noteuspto-grants-2012_10