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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443763Generated: October 27, 2026

Acetone → 3-[4-Chloro-6-(1,1,3,3-tetramethylbutylamino)-s-triazin-2-yl]-3-azabicyclo[3.2.2]nonane

https://huagongshe.com/reaction/443763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium HydroxideHCID 14798—
Reactanttert-OctylamineHCID 61017—
Reactant3-(4,6-Dichloro-s-triazin-2-yl)-3-azabicyclo[3.2.2]nonaneHCID 15572579—
SolventWaterHCID 962—
Product3-[4-Chloro-6-(1,1,3,3-tetramethylbutylamino)-s-triazin-2-yl]-3-azabicyclo[3.2.2]nonaneHCID 15572580—

Reaction Steps

Thirty grams (0.11 mole) of 3-(4,6-dichloro-s-triazin-2-yl)-3-azabicyclo[3.2.2]nonane is dissolved in 300 ml. of acetone and then 370 ml. of water is added followed by 20 g. (0.15 mole) of tert-octylamine. After stirring for 10 minutes, 4.4 g. (0.11 mole) of NaOH in 30 ml. of water is added over 20 minutes. The reaction is then heated to reflux for 19 hours. After cooling to room temperature, one liter of water is added, stirred for one hour and the white precipitate filtered off. The precipitate is washed with water, dried overnight, dissolved in dichloromethane and filtered through Magnesol®. The Magnesol® is then washed with dichloromethane, solvent removed in vacuo and recrystallized from dichloromethane-hexanes giving 20 g. of colorless crystals, m.p. 159°-162.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261892
Source datasetuspto-grants-1981_04
ORD IDord-66194526f06b4de2bcb4624a4b33bb40
Source noteuspto-grants-1981_04