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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846246Generated: October 26, 2026

Acetonitrile → Triphenylphosphine

https://huagongshe.com/reaction/846246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTetrahydrofuranHCID 8028—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 178514248HCID 178514248—
SolventCarbon TetrachlorideHCID 5943—
SolventChloroformHCID 6212—
ProductTriphenylphosphineHCID 11776—
ProductOxazolineHCID 68157—

Reaction Steps

Hydroxyamide IX is then subjected to cyclodehydration in an inert organic solvent (e.g., tetrahydrofuran, acetonitrile or chloroform) under an inert atmosphere (e.g., argon) with triphenylphosphine (employing a molar ratio of V:triphenylphosphine of from about 0.8:1 to about 1:1) and carbon tetrachloride in the presence of an amine base (e.g., triethylamine or diisopropylethylamine) to form oxazoline ##STR23##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05135939
Source datasetuspto-grants-1992_08
ORD IDord-9faeadff4ef440cda5bbff849c7c2f54
Source noteuspto-grants-1992_08