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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46654Generated: October 30, 2026

Hydrogen Sulfide → Triarathene

https://huagongshe.com/reaction/46654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
Reactant1,4-Butanedione, 4-(4-chlorophenyl)-1,2-diphenyl-HCID 11325522—
SolventEthanolHCID 702—
SolventO-XyleneHCID 7237—
ProductTriaratheneHCID 6450825134.7%

Reaction Steps

In a 1-liter stainless steel autoclave equipped with stirrer were placed 76.9 g (0.220 mole) of 1,2-diphenyl4-p-chlorophenylbutane-1,4-dione, 100 ml of xylene and 45 g (0.101 mole) of phosphorus pentasulfide. The autoclave was cooled with a Dry Ice-acetone bath and charged with 120 g (3.52 moles) of hydrogen sulfide. The autoclave was heated with stirring for 200 minutes at 155°-178° C. (1000-2000 psig). The autoclave was cooled and the hydrogen sulfide allowed to escape into a sodium hydroxide solution. The residue was stirred with 150 ml of absolute ethanol. Filtration and drying gave a crude product of 61.2 g (80.2%) m.p. 115°-117°. Recrystallization from 190 ml of toluene and 625 ml of ethanol gave 47.2 g (61.9%) of pure 2,3-diphenyl-5-p-chlorophenylthiophene, m.p. 121°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174405
Source datasetuspto-grants-1979_11
ORD IDord-3023d7c751fc477492f211786f8263c2
Source noteuspto-grants-1979_11