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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285209Generated: October 27, 2026

Pyridine → 8-Azabicyclo[3.2.1]octane-8-carbonyl chloride

https://huagongshe.com/reaction/2285209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriphosgeneHCID 94429—
Reactant8-Azabicyclo(3.2.1)octaneHCID 136097—
SolventDichloromethaneHCID 6344—
Product8-Azabicyclo[3.2.1]octane-8-carbonyl chlorideHCID 1224753570.3%

Reaction Steps

To a cooled (10° C.) solution 8-aza-bicyclo[3.2.1]octane (295 mg, 2.00 mmol) and pyridine (486 μL, 6.02 mmol) in DCM (10 mL) was added triphosgene (595 mg, 2.00 mmol) portionwise. The reaction was allowed to reach room temperature and stirred overnight. The mixture was quenched with HCl (1M aqueous, 10 mL) and stirred for 30 min. The aqueous phase was extracted with DCM (×3) and the combined organic layers were washed with HCl (1M aqueous), brine, dried (MgSO4) and concentrated in vacuo, to give the title compound (244 mg, 70%). 1H NMR (400 MHz, CDCl3): 1.46-1.70 (4H, m), 1.72-1.92 (5H, m), 2.04-2.11 (2H, m), 4.39-4.44 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145413B2
Source datasetuspto-grants-2015_09
ORD IDord-f0c215029a95466d8ac741265719df84
Source noteuspto-grants-2015_09