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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172352Generated: October 31, 2026

Triphenylphosphine → Phosphonium, (5-hydroxypentyl)triphenyl-, bromide

https://huagongshe.com/reaction/2172352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-Pentanol, 5-bromo-HCID 118709—
SolventEthanolHCID 702—
ProductPhosphonium, (5-hydroxypentyl)triphenyl-, bromideHCID 2784772—

Reaction Steps

An equivalent of 5-bromopentanol and an equivalent of triphenylphosphine in refluxed ethanol are placed in a flask. After 72 hours of agitation in these conditions, and once returned to ambient temperature, the ethanol is evaporated under vacuum and the residue is placed into toluene at 4° C. overnight. The (5-hydroxypentyl)triphenylphosphonium bromide formed is filtered on a frit, rinsed with methyl tert-butyl ether then dried under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051531B2
Source datasetuspto-grants-2015_06
ORD IDord-a220f2c9520343af94c86a165878c8c8
Source noteuspto-grants-2015_06