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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697371Generated: November 1, 2026

Boron trifluoride etherate → 1-(2-(Benzyloxy)-5-fluorophenyl)cyclopropanamine

https://huagongshe.com/reaction/1697371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant2-(Benzyloxy)-5-fluorobenzonitrileHCID 58281472—
ReactantHCID 178418443HCID 178418443—
CatalystTitanium isopropoxideHCID 11026—
SolventDiethyl EtherHCID 3283—
Product1-(2-(Benzyloxy)-5-fluorophenyl)cyclopropanamineHCID 66688931—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Ethylmagnesium bromide, (35.2 ml of a 3M solution in diethyl ether) was added as a slow stream to a mechanically stirred mixture of tetraisopropyl orthotitanate (16.37 mL) and 2-(benzyloxy)-5-fluorobenzonitrile (12 g) in diethyl ether (400 mL) cooled to −78° C. The resulting solution was stirred at −78° C. for 15 min and then warmed to room temperature over 1.5 h. Boron trifluoride etherate (13.38 mL) was added and the mixture was stirred for 30 min. The reaction was quenched with 1 M HCl (400 ml) and the aqueous layer was separated. The diethyl ether layer was further extracted into 1M HCl (2×200 mL). The combined aqueous layers were cooled in an ice bath and basified with 1M aqueous NaOH solution. The resulting precipitate was filtered through celite washing the pad extensively with water (200 mL), dichloromethane (4×200 mL) then dichloromethane/MeOH (90:10, 300 mL). The combined filtrates were separated and the aqueous layer further extracted into dichloromethane (2×200 mL). The combined organics were dried (MgSO4) and evaporated and residue purified by SCX resin (eluting with methanol followed by 10% 880 ammonia in methanol). The basic fractions were evaporated to give the subtitle compound (3.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163905B2
Source datasetuspto-grants-2012_04
ORD IDord-52030cf2818b4e60a4fc6d4e0d1f88fb
Source noteuspto-grants-2012_04