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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468371Generated: October 26, 2026

2-Aminobenzyl alcohol → (2-Aminobenzyl)triphenylphosphonium bromide

https://huagongshe.com/reaction/468371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminobenzyl alcoholHCID 21439—
ReactantTriphenylphosphonium bromideHCID 80811—
SolventAcetonitrileHCID 6342—
Product(2-Aminobenzyl)triphenylphosphonium bromideHCID 1096131588.4%

Reaction Steps

2-Aminobenzyl alcohol (60.0 g, 0.487 mol) was dissolved in acetonitrile (2.5 L) and brought to reflux. Triphenylphosphine hydrobromide (167 g, 0.487 mol) was added and the mixture was heated at reflux for 3 h. The reaction mixture was concentrated to approximately 500 mL and left at room temperature for 1 h. The precipitate was filtered and washed with cold acetonitrile followed by hexane. The solid was dried overnight at 40° C. under vacuum to give triphenyl(2-aminobenzyl)phosphonium bromide (193 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623905B2
Source datasetuspto-grants-2014_01
ORD IDord-d3c011fa54dc49abb7ffd437c3a653c8
Source noteuspto-grants-2014_01