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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427593Generated: October 31, 2026

Boron trifluoride etherate → HCID 86701035, compound

https://huagongshe.com/reaction/1427593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantHCID 10535529HCID 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 (3-M 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-butyldim ethylsilyloxy)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 numberUS08933232B2
Source datasetuspto-grants-2015_01
ORD IDord-daf87c02bc5442b0988903266864819e
Source noteuspto-grants-2015_01