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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54153Generated: October 30, 2026

Pyridine → HCID 53762272, compound

https://huagongshe.com/reaction/54153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant[1-(2,3-Dimethoxybenzyl)cycloheptyl]methanolHCID 19961173—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 53762272HCID 5376227281%

Reaction Steps

The alcohol from Step C above (25 g, 89 mmol) was dissolved in 500 mL of anhydrous DMSO. To this solution was added Et3N (50 mL, 358 mmol). Then SO3.Pyridine (57 g, 358 mmol), was dissolved in 400 mL of DMSO, and this solution was added to the reaction vessel. The solution was then stirred at room temperature for two hours. The reaction solution was then poured over ice and the resulting mixture was warmed to room temperature and extracted with CH2Cl2. The organic layer was washed with 1M HCl, water, and brine, then the organic layer was dried over MgSO4, filtered and evaporated. The crude product was chromatographed on silica gel, eluting with 10:1 hexane:EtOAc to give the title product as a colorless oil (20 g, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05621133
Source datasetuspto-grants-1997_04
ORD IDord-34ae82ec46294e1f90e675899fae7f5e
Source noteuspto-grants-1997_04