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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | Tetraphosphorus nonasulfide | HCID 141172 | — |
| Reactant | 1-Cyano-1-hydroxy-1-(4-isobutylphenyl)ethane | HCID 15628327 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4-Isobutylphenyl)propiononitrile | HCID 108374 | — |
| Product | 2-(4-Isobutylphenyl)acrylonitrile | HCID 13227708 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04952718 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-73bc2067b2d44290b2659aad313c6a6a |
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| Source note | uspto-grants-1990_08 |
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