Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360022Generated: October 25, 2026

Toluene → 2-(Benzyloxy)-6-(pyrrolidin-1-yl)pyridine

https://huagongshe.com/reaction/1360022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPyrrolidineHCID 31268—
Reactant2-Benzyloxy-6-bromopyridineHCID 817475—
ReactantSodium t-butoxideHCID 23676156—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventEthyl AcetateHCID 8857—
Product2-(Benzyloxy)-6-(pyrrolidin-1-yl)pyridineHCID 6697010892.4%

Reaction Steps

In a dried microwave reactor into which an argon gas was introduced, 526 mg (2.0 mmol) of 2-(benzyloxy)-6-bromopyridine, 200 μl (2.4 mmol) of pyrrolidine, 283 mg (2.8 mmol) of sodium t-butoxide, 9 mg (0.005 mmol) of tris(dibenzylideneacetone)dipalladium(O) (0.5 mol % of Pd), 19 mg (0.015 mmol, 1.5 mol %) of (±)-BINAP and 3 ml of toluene were placed, followed by stirring and reacting the mixture using microwave at 120° C. for 10 min. The reaction mixture was diluted with 20 ml of ethyl acetate, filtered through Cellite, and kept under a reduced pressure to remove the solvent. The residue was subjected to column chromatography using 10% ethyl acetate/hexane as an eluent to obtain 470 mg (yield 92%) of 2-(benzyloxy)-6-(pyrrolidin-1-yl)pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879835B2
Source datasetuspto-grants-2011_02
ORD IDord-f8aed5c7fff54172af91d4331e760ed4
Source noteuspto-grants-2011_02