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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238541Generated: October 26, 2026

Hydrochloric Acid → {[2-Chloro-4-fluoro-3-(trifluoromethyl)phenyl]methyl}amine hydrochloride

https://huagongshe.com/reaction/2238541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantBoraneHCID 6331—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Chloro-4-fluoro-3-(trifluoromethyl)benzamideHCID 67460657—
SolventWaterHCID 962—
Product{[2-Chloro-4-fluoro-3-(trifluoromethyl)phenyl]methyl}amine hydrochlorideHCID 8661753878.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Chloro-4-fluoro-3-(trifluoromethyl)benzamide (0.490 g, 2.03 mmol) was treated with 1M borane in tetrahydrofuran (20.33 ml, 20.33 mmol) and stirred at 60° C. overnight. The mixture was then treated with 2N aqueous hydrogen chloride until gas evolution ceased and then stirred at 100° C. for 2 hrs. The mixture was reduced in vacuo and the residue was taken up in a minimum of water and washed with dichloromethane (30 ml). The pH of the aqueous layer was adjusted to pH11 by the addition of 2N aqueous sodium hydroxide solution and then extracted with dichloromethane (2×25 ml). The dichloromethane layers were separated using a hydrophobic frit, combined and evaporated in vacuo to leave a pale yellow oil. A 1M solution of hydrogen chloride in diethyl ether (3 ml, 3 mmol) was added and the resulting white solid was filtered off to give pure {[2-Chloro-4-fluoro-3-(trifluoromethyl)phenyl]methyl}amine hydrochloride (0.210 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718693B2
Source datasetuspto-grants-2010_05
ORD IDord-c8a4ee171d6c411e8debc9a7d3a106f4
Source noteuspto-grants-2010_05