Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427658Generated: November 2, 2026

Boron trifluoride etherate → HCID 86701035, compound

https://huagongshe.com/reaction/1427658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant3-((tert-Butyldimethylsilyl)oxy)propanenitrileHCID 10535529—
ReactantHCID 178418443HCID 178418443—
CatalystTitanium isopropoxideHCID 11026—
SolventDiethyl EtherHCID 3283—
ProductHCID 86701035HCID 8670103530%

Reaction Steps

To a solution of 3-(tert-butyldimethylsilyloxy)propanenitrile (11.1 g, 60 mmol) in Et2O (400 mL) was added titanium tetraisopropanolate (28.9 g, 102 mmol) under N2 atmosphere. Ethylmagnesium bromide (3M in Et2O, 50 mL) was slowly added drop-wise at 0° C. The mixture was stirred at rt for 1 hr. Boron trifluoride etherate (17.0 g, 120 mmol) was slowly added at 0° C. The mixture was stirred at rt for 1 hr. The mixture was quenched with 10% aq. NaOH (300 mL) and then extracted with DCM (3×). The combined organic layer was dried over Na2SO4 and concentrated. The residue was purified by silica gel column chromatography (gradient elution 5˜50% EtOAc/petroleum ether) to afford 1-(2-(tert-butyldimethylsilyloxy)ethyl)cyclopropanamine (3.9 g, 30%) as a colorless oil. ESI-MS (EI+, m/z): 216.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933233B2
Source datasetuspto-grants-2015_01
ORD IDord-df18ee863f9847438b75f6b4d99fc63f
Source noteuspto-grants-2015_01