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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404452Generated: October 29, 2026

Cyanuric chloride → 3-(4,6-Dichloro-1,3,5-triazin-2-yl)-8-oxa-3-azabicyclo[3.2.1]octane

https://huagongshe.com/reaction/404452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
Reactant8-Oxa-3-aza-bicyclo(3.2.1)octane hydrochlorideHCID 21983536—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventSodium BicarbonateHCID 516892—
Product3-(4,6-Dichloro-1,3,5-triazin-2-yl)-8-oxa-3-azabicyclo[3.2.1]octaneHCID 5796824760.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of cyanuric chloride (2.00 g, 10.85 mmoles) in acetone (20 mL) and water (10 mL) at 0° C. was added a solution of 8-oxa-3-azabicyclo[3.2.1]octane hydrochloride (1.46 g, 9.76 mmoles) in saturated aqueous NaHCO3 (25 mL) and acetone (25 mL) via addition funnel over 15 minutes. The reaction was stirred at 0° C. for 2 hours, then filtered to collect a white precipitate. The precipitate was washed with water (25 mL) and dried. The crude product was purified by column chromatography (30:70 ethyl acetate in hexanes) to provide 3-(4,6-dichloro-1,3,5-triazin-2-yl)-8-oxa-3-azabicyclo[3.2.1]octane (1.55 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748421B2
Source datasetuspto-grants-2014_06
ORD IDord-8db4ba9f2bb947f4adb1f114605df31d
Source noteuspto-grants-2014_06