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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710211Generated: October 25, 2026

Phosphorus sulfide (P2S5) → 2-(4-Isobutylphenyl)propiononitrile

https://huagongshe.com/reaction/1710211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantTetraphosphorus nonasulfideHCID 141172—
Reactant1-Cyano-1-hydroxy-1-(4-isobutylphenyl)ethaneHCID 15628327—
SolventTolueneHCID 1140—
Product2-(4-Isobutylphenyl)propiononitrileHCID 108374—
Product2-(4-Isobutylphenyl)acrylonitrileHCID 13227708—

Reaction Conditions

Temperature85 °C

Reaction Steps

A crude solution of 410 mg (2.0 mmol) of 1-cyano-1-hydroxy-1-(4-isobutylphenyl)ethane (IBACH) in 5 mL of toluene was treated under nitrogen with 450 mg (1.0 mmol) of a finely-ground commercial phosphorus pentasulfide which is a mixture of tetraphosphorus decasulfide and tetraphosphorus nonasulfide. The reaction mixture was stirred well and heated in an 85° C. bath for one hour. GC analysis of the crude reaction product indicated that the reaction resulted in the formation of 1-cyano-1-(4-isobutylphenyl)ethane (PN) and 2-(4-isobutylphenyl)acrylonitrile (UN) in a ratio of 2/1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952718
Source datasetuspto-grants-1990_08
ORD IDord-73bc2067b2d44290b2659aad313c6a6a
Source noteuspto-grants-1990_08