Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743695Generated: October 31, 2026

Sodium Iodide → 3-Allyl-8-benzyl-3,8-diazabicyclo[3.2.1]octane

https://huagongshe.com/reaction/1743695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAllylamineHCID 7853—
ReactantSodium BicarbonateHCID 516892—
ReactantCis-1-benzyl-2,5-bis(chloromethyl)pyrrolidine hydrochlorideHCID 22940372—
SolventAcetonitrileHCID 6342—
Product3-Allyl-8-benzyl-3,8-diazabicyclo[3.2.1]octaneHCID 2223558998.7%

Reaction Steps

Allylamine (9.5 mL, 0.13 mol) was added to a suspension of cis-1-benzyl-2,5-bis(chloromethyl)pyrrolidine hydrochloride (37.5 g, 0.13 mol, from step (e) above), NaI (47.6 g, 0.32 mol) and NaHCO3 (106.7 g, 1.27 mol) in acetonitrile (1.8 L). The reaction was heated at reflux for 8 h, filtered, and the filtrate concentrated in vacuo. The residue was partitioned between ethyl acetate and ice cold 1 N NaOH. The ethyl acetate layer was separated, dried (Na2SO4), filtered and concentrated in vacuo to afford 31.1 g of an oil. The oil was chromatographed on a column of silica (75 mm×220 mm) eluting with a mixture of chloroform, methanol and conc. NH4OH (240:9:1). Fractions (100 mL each) 5–10 were combined and concentrated in vacuo to afford 22.2 g (72%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012074B2
Source datasetuspto-grants-2006_03
ORD IDord-03e0cefb5d4c4905bea7fec2d9619c0b
Source noteuspto-grants-2006_03