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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46662Generated: October 29, 2026

Hydrogen Sulfide → 2,3-Diphenyl-5-p-methoxyphenylthiophene

https://huagongshe.com/reaction/46662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantO-XyleneHCID 7237—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
Reactant1,2-Diphenyl-4-p-methoxyphenylbutane-1,4-dioneHCID 2733039—
SolventEthanolHCID 702—
Product2,3-Diphenyl-5-p-methoxyphenylthiopheneHCID 54091294142.8%

Reaction Steps

In a 1-liter steel autoclave fitted with a mechanical stirrer, a thermometer and a pressure gauge were placed 32 g (0.09 mole) of 1,2-diphenyl-4-p-methoxyphenylbutane-1,4-dione, 100 ml of xylene, 20 g (0.045 mole) of phosphorus pentasulfide and 130 g of hydrogen sulfide. The mixture was stirred and heated 3 hours at 157°-162° C. (1190-1220 psig). The vessel was cooled and the hydrogen sulfide vented into an aqueous sodium hydroxide trap. The semisolid residue was stirred with 150 ml of absolute ethanol. Filtration gave 23 g (72%) of crude product, m.p. 130°-132° C. and a second crop of 3.7 g (11.6%) m.p. 124°-126° C. The two crops were combined and recrystallized from a mixture of 30 ml of dioxane and 60 ml of absolute ethanol to give 22 g (69%) of pure product m.p. 133°-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174405
Source datasetuspto-grants-1979_11
ORD IDord-3d4393c5c73f41ff80a02d1f48faa88f
Source noteuspto-grants-1979_11