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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054368Generated: November 1, 2026

Borane → 2-(4-Bromo-phenoxy)-propylamine

https://huagongshe.com/reaction/1054368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
ReactantTetrahydrofuranHCID 8028—
Reactant2-(4-bromophenoxy)propanamideHCID 2953581—
SolventMethanolHCID 887—
Product2-(4-Bromo-phenoxy)-propylamineHCID 22388589—

Reaction Steps

A 1 M solution of borane in tetrahydrofuran (8.2 ml, 8.2 mmol) was added dropwise to 2-(4-bromo-phenoxy)-propionamide (0.2 g, 0.82 mmol) and the solution was stirred overnight at reflux then subsequently hydrolysed by slow addition of excess of methanol and refluxing for a further 2 hours. The solvent was removed under reduced pressure and aqueous ammonium chloride was added. The aqueous phase was extracted twice with ethyl acetate and the organics were combined, dried over anhydrous magnesium sulfate and concentrated in vacuo to give the desired product. Yield 0.13 g, 68%. LCMS method: 2, RT: 2.74 min; MI: 271-273 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394301B2
Source datasetuspto-grants-2016_07
ORD IDord-8e88fb0ab6cf489bae071518bac2591b
Source noteuspto-grants-2016_07