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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526537Generated: October 29, 2026

Boron trifluoride etherate → HCID 90389378, compound

https://huagongshe.com/reaction/1526537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant2-Fluoro-6-iodotolueneHCID 2774523—
ReactantHCID 90389379HCID 90389379—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 90389378HCID 9038937844.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a flame dried RBF was added a solution of n-butyllithium (2.5M in hexanes; 3.01 ml, 7.51 mmol) and diethyl ether (15 ml). The solution was cooled to −78° C., and 2-fluoro-6-iodotoluene (0.981 ml, 7.51 mmol) was added dropwise and the reaction was stirred at −78° C. for 10 minutes. A −78° C. premixed solution of 4-(difluoromethyl)-2-oxa-3-azabicyclo[3.1.0]hex-3-ene (1.00 g, 7.51 mmol) and boron trifluoride diethyl etherate (0.927 ml, 7.51 mmol) in toluene (10 ml) was added to the reaction via syringe. The reaction was stirred at −78° C. for 10 minutes, quenched with saturated ammonium chloride and warmed to RT. The reaction was diluted with water and EtOAc. The organic layer was separated and concentrated under reduced pressure. The crude residue was purified via silica gel flash chromatography eluting with 0-20% ethyl acetate in hexanes to afford 4-(difluoromethyl)-4-(3-fluoro-2-methylphenyl)-2-oxa-3-azabicyclo[3.1.0]hexane (0.81 g, 3.33 mmol, 44.3% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085576B2
Source datasetuspto-grants-2015_07
ORD IDord-751ee9ac6048454598ede3d7cb0a2275
Source noteuspto-grants-2015_07