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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218569Generated: October 25, 2026

Azobisisobutyronitrile → 4-Acetylthio-1,1-bis(trifluoromethyl)-1-butanol

https://huagongshe.com/reaction/2218569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
Reactant4-Penten-2-ol, 1,1,1-trifluoro-2-(trifluoromethyl)-HCID 328870—
ReactantHCID 178418634HCID 178418634—
CatalystAzobisisobutyronitrileHCID 6547—
Solvent1,4-DioxaneHCID 31275—
Product4-Acetylthio-1,1-bis(trifluoromethyl)-1-butanolHCID 8659429880%

Reaction Steps

Under a nitrogen atmosphere, 20 g of 4,4-bis(trifluoromethyl)-4-hydroxy-1-butene (96.1 mmol), 8.05 g of thioacetic acid (105.7 mmol), 60 g of 1,4-dioxane and 0.79 g of 2,2′-azobisisobutyronitrile (hereinafter abbreviated as AIBN) (4.8 mmol) were put into a flask equipped with a stirring bar, a thermometer and a condenser, and heated with stirring. During the reaction, thioacetic acid and AIBN were appropriately added and after confirming that a substrate was completely consumed, the reaction solution was distilled as it was under reduced pressure to yield an intermediate product, 22 g of 4-acetylthio-1,1-bis(trifluoromethyl)-1-butanol (76.9 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07411097B2
Source datasetuspto-grants-2008_08
ORD IDord-eb970c3d5fb043828d0f48b16c0cc4b5
Source noteuspto-grants-2008_08