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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46657Generated: October 29, 2026

Hydrogen Sulfide → 2,3-Diphenyl-5-m-anisylthiophene

https://huagongshe.com/reaction/46657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantHCID 20386701HCID 20386701—
SolventCarbon DioxideHCID 280—
SolventEthanolHCID 702—
SolventO-XyleneHCID 7237—
Product2,3-Diphenyl-5-m-anisylthiopheneHCID 2038666482.3%

Reaction Steps

In a 1-liter stainless steel autoclave equipped with stirrer were placed 51.6 g (0.150 mole) of 1,2-diphenyl-4-m-anisylbutane-1,4-dione, 100 ml of xylene and 30 g (0.0675 mole) of phosphorus pentasulfide. The autoclave was cooled in Dry Ice and charged with 130 g (3.81 moles) of hydrogen sulfide. The mixture was then heated and stirred 235 minutes at 154°-177° C. (1120-1320 psig). The vessel was cooled to room temperature. The hydrogen sulfide was vented into a sodium hydroxide solution. The residue was treated with 150 ml of absolute ethanol to destroy excess phosphorus sulfides. Washing the product with another 330 ml of ethanol gave 32 g (62.3%) of crude product. Recrystallization from 50 ml of toluene and 150 ml of ethanol gave 19.8 g (38.5%) of pure 2,3-diphenyl-5-m-anisylthiophene, m.p. 100°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174405
Source datasetuspto-grants-1979_11
ORD IDord-c97a814917c94e0094771d1c78b58c6e
Source noteuspto-grants-1979_11