Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46655Generated: October 29, 2026

Hydrogen Sulfide → 2,3-Di-p-anisyl-5-p-tolylthiophene

https://huagongshe.com/reaction/46655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantHCID 57279740HCID 57279740—
SolventEthanolHCID 702—
SolventO-XyleneHCID 7237—
Product2,3-Di-p-anisyl-5-p-tolylthiopheneHCID 20386672—

Reaction Steps

In a 1-liter stainless steel autoclave equipped with stirrer were placed 40.6 g (0.105 mole) of 1,2-di-p-anisyl-4-p-tolylbutene-1,4-dione, 100 ml of xylene and 25 g (0.056 mole) of phosphorus pentasulfide. The vessel was chilled with a Dry Ice-acetone bath and charged with 130 g (3.81 moles) of hydrogen sulfide. The autoclave was then heated with stirring for 215 minutes at 158°-165° C. (1250-1360 psig). After cooling the vessel, the hydrogen sulfide was allowed to vent into a sodium hydroxide solution. The residue was treated with 150 ml of absolute ethanol to destroy unreacted phosphorus pentasulfide. After removal of the ethanol there remained 70.5 g of crude product. Recrystallization from ethanol-dioxane (70:30) gave 20 g (49.3%) of pure 2,3-di-p-anisyl-5-p-tolythiophene, m.p. 99°-102° C. and a second crop of 6.5 g (16.0%) m.p. 92°-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174405
Source datasetuspto-grants-1979_11
ORD IDord-cbf44bfcc2da40f6a16f47af255540fa
Source noteuspto-grants-1979_11