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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405511Generated: October 29, 2026

Borane → 3-(2-Bromophenyl)-1-propanamine

https://huagongshe.com/reaction/1405511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
Reactant3-(2-Bromophenyl)propanenitrileHCID 13308298—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Bromophenyl)-1-propanamineHCID 12413906—

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 250-mL 3-necked round-bottom flask, was placed a solution of 3-(2-bromophenyl)propanenitrile (2.1 g, 10.00 mmol, 1.00 equiv) in tetrahydrofuran (20 mL). This was followed by the addition of borane (1 mol/L in THF, 50 mL, 5.00 equiv) dropwise with stirring at 0° C. The resulting solution was stirred for overnight at room temperature. The reaction was then quenched by the addition of 50 mL of water at 0° C. and extracted with 3×50 mL of ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was dissolved in 30 mL of 6N aqueous hydrogen chloride. The aqueous solution was extracted with 30 mL of ethyl acetate and the aqueous layers were combined. The pH value of the aqueous solution was adjusted to 10 with 10% aqueous sodium hydroxide. The resulting solution was extracted with 3×50 mL of ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate, concentrated under vacuum. This resulted in 1.3 g (58%) of 3-(2-bromophenyl)propan-1-amine as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916560B2
Source datasetuspto-grants-2014_12
ORD IDord-44687d8fa55a4f3c841beb9cefd5d09c
Source noteuspto-grants-2014_12