Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606781Generated: October 25, 2026

Triglyme → 3-(p-Chlorophenethyl)-8-oxa-3-azabicyclo(3.2.1)octane

https://huagongshe.com/reaction/1606781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriglymeHCID 8189—
ReactantSodium HydroxideHCID 14798—
Reactant2-(4-Chlorophenyl)ethylamineHCID 67430—
Reactant(Tetrahydrofuran-2,5-diyl)bis(methylene) bis(4-methylbenzenesulfonate)HCID 259634—
Product3-(p-Chlorophenethyl)-8-oxa-3-azabicyclo(3.2.1)octaneHCID 21544555—

Reaction Conditions

Temperature180 °C

Reaction Steps

p-Chlorophenethylamine (0.643 mole, 100 grams) was added to a mixture of 2,5-bis(tosyloxymethyl)tetrahydrofuran (0.214 mole, 99.6 grams) and 200 ml of Ansul 161 (triethylene glycol dimethyl ether) and stirred the reaction mixture for 3 hours at 180° C. The reaction mixture was cooled to room temperature and neutralized with a methanolic sodium hydroxide solution (0.429 mole, 17.14 grams NaOH in 200 ml CH3OH) while stirring for 15 minutes. The solvents and excess starting amine were distilled from the reaction mixture under aspirator pressure. The residue was filtered collecting the sodium p-toluenesulfonate. The filtrate was distilled collecting one fraction (terminal pot temperature 280° C./0.1 mm Hg). The distillate which solidified was recrystallized from methanol obtaining 3-(p-chlorophenethyl)-8-oxa-3-azabicyclo(3.2.1)octane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953596
Source datasetuspto-grants-1976_04
ORD IDord-d58de6d27fe040538899deb8fcb4ce27
Source noteuspto-grants-1976_04