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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405573Generated: October 31, 2026

2-(2-bromophenoxy)acetonitrile → 2-(2-Bromophenoxy)ethan-1-amine

https://huagongshe.com/reaction/1405573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-bromophenoxy)acetonitrileHCID 2734208—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Bromophenoxy)ethan-1-amineHCID 22688745—

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 500-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 2-(2-bromophenoxy)acetonitrile (5.63 g, 26.68 mmol, 1.00 equiv) in tetrahydrofuran (20 mL). This was followed by the addition of BH3 in tetrahydrofuran (143 mL, 5.30 equiv) dropwise with stirring at 0° C. The resulting solution was stirred overnight at 20° C. in an oil bath and quenched by the addition of water (10 ml). The resulting mixture was concentrated under vacuum and diluted with water. The pH value of the aqueous solution was adjusted to 10 with 1N sodium hydroxide and extracted with 6×50 mL of dichloromethane. The organic layers was combined and concentrated under vacuum. This resulted in 5.67 g (crude) of 2-(2-bromophenoxy)ethanamine as pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916560B2
Source datasetuspto-grants-2014_12
ORD IDord-c1751887049642e4942835d49a465830
Source noteuspto-grants-2014_12