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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877693Generated: October 30, 2026

Boron trifluoride etherate → 1-(furan-2-yl)cyclopropanaMine

https://huagongshe.com/reaction/1877693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium HydroxideHCID 14798—
Reactant2-FuronitrileHCID 69245—
ReactantHCID 178461630HCID 178461630—
CatalystTitanium isopropoxideHCID 11026—
SolventTetrahydrofuranHCID 8028—
Product1-(furan-2-yl)cyclopropanaMineHCID 56773733—

Reaction Steps

To a solution of 2-furonitrile (5 g, 53.71 mmol, 1.0 eq) in dry THF under an argon atmosphere was added slowly titanium isopropoxide (18.9 ml, 64.4 mmol, 1.2 eq) at r.t. The reaction mixture was stirred for 15 min. A 1M solution of EtMgBr in THF (129 ml, 129 mmol, 2.4 eq) was added slowly via syringe to the mixture at 0° C. After addition, the reaction mixture was allowed to warm to r.t. and stirred at r.t. for 2 hour. BF3.Et2O (10.4 ml) was then added slowly to the mixture at 0° C. After the completion of addition, the reaction mixture was stirred at r.t. for 30 min. The reaction mixture was added with ice, and then with 10% NaOH solution slowly till the reaction mixture becomes basic. The mixture was extracted with EtOAc. The organic was washed with brine, dried over Na2SO4 and concentrated. The crude product was purified by silica gel (60-120) column chromatography using 35% EtOAc/Pet ether as eluent. Yield: 2.5 g (crude).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309558B2
Source datasetuspto-grants-2012_11
ORD IDord-912cc34b7fbb4c26a4c4d912313e46a1
Source noteuspto-grants-2012_11